GSM3215617: scATAC-D0-10; Homo sapiens; ATAC-seq

SRX4301970 GSM3215617 GSM3215617: scATAC-D0-10; Homo sapiens; ATAC-seq SRP151379 SRS3467377 GSM3215617 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215617 GSM3215617 GEO Accession GSM3215617 SRX4301971 GSM3215618 GSM3215618: scATAC-D0-11; Homo sapiens; ATAC-seq SRP151379 SRS3467375 GSM3215618 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215618 GSM3215618 GEO Accession GSM3215618 SRX4301972 GSM3215619 GSM3215619: scATAC-D0-12; Homo sapiens; ATAC-seq SRP151379 SRS3467379 GSM3215619 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215619 GSM3215619 GEO Accession GSM3215619 SRX4301973 GSM3215620 GSM3215620: scATAC-D0-13; Homo sapiens; ATAC-seq SRP151379 SRS3467454 GSM3215620 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215620 GSM3215620 GEO Accession GSM3215620 SRX4301974 GSM3215621 GSM3215621: scATAC-D0-14; Homo sapiens; ATAC-seq SRP151379 SRS3467376 GSM3215621 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215621 GSM3215621 GEO Accession GSM3215621 SRX4301975 GSM3215622 GSM3215622: scATAC-D0-15; Homo sapiens; ATAC-seq SRP151379 SRS3467378 GSM3215622 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215622 GSM3215622 GEO Accession GSM3215622 SRX4301976 GSM3215623 GSM3215623: scATAC-D0-16; Homo sapiens; ATAC-seq SRP151379 SRS3467382 GSM3215623 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215623 GSM3215623 GEO Accession GSM3215623 SRX4301977 GSM3215624 GSM3215624: scATAC-D0-17; Homo sapiens; ATAC-seq SRP151379 SRS3467380 GSM3215624 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215624 GSM3215624 GEO Accession GSM3215624 SRX4301978 GSM3215625 GSM3215625: scATAC-D0-18; Homo sapiens; ATAC-seq SRP151379 SRS3467384 GSM3215625 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215625 GSM3215625 GEO Accession GSM3215625 SRX4301979 GSM3215626 GSM3215626: scATAC-D0-19; Homo sapiens; ATAC-seq SRP151379 SRS3467383 GSM3215626 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215626 GSM3215626 GEO Accession GSM3215626 SRX4301980 GSM3215627 GSM3215627: scATAC-D0-1; Homo sapiens; ATAC-seq SRP151379 SRS3467381 GSM3215627 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215627 GSM3215627 GEO Accession GSM3215627 SRX4301981 GSM3215628 GSM3215628: scATAC-D0-20; Homo sapiens; ATAC-seq SRP151379 SRS3467385 GSM3215628 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215628 GSM3215628 GEO Accession GSM3215628 SRX4301982 GSM3215629 GSM3215629: scATAC-D0-21; Homo sapiens; ATAC-seq SRP151379 SRS3467386 GSM3215629 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215629 GSM3215629 GEO Accession GSM3215629 SRX4301983 GSM3215630 GSM3215630: scATAC-D0-22; Homo sapiens; ATAC-seq SRP151379 SRS3467466 GSM3215630 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215630 GSM3215630 GEO Accession GSM3215630 SRX4301984 GSM3215631 GSM3215631: scATAC-D0-23; Homo sapiens; ATAC-seq SRP151379 SRS3467486 GSM3215631 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215631 GSM3215631 GEO Accession GSM3215631 SRX4301985 GSM3215632 GSM3215632: scATAC-D0-24; Homo sapiens; ATAC-seq SRP151379 SRS3467465 GSM3215632 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215632 GSM3215632 GEO Accession GSM3215632 SRX4301986 GSM3215633 GSM3215633: scATAC-D0-25; Homo sapiens; ATAC-seq SRP151379 SRS3467387 GSM3215633 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215633 GSM3215633 GEO Accession GSM3215633 SRX4301987 GSM3215634 GSM3215634: scATAC-D0-26; Homo sapiens; ATAC-seq SRP151379 SRS3467392 GSM3215634 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215634 GSM3215634 GEO Accession GSM3215634 SRX4301988 GSM3215635 GSM3215635: scATAC-D0-27; Homo sapiens; ATAC-seq SRP151379 SRS3467439 GSM3215635 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215635 GSM3215635 GEO Accession GSM3215635 SRX4301989 GSM3215636 GSM3215636: scATAC-D0-28; Homo sapiens; ATAC-seq SRP151379 SRS3467388 GSM3215636 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215636 GSM3215636 GEO Accession GSM3215636 SRX4301990 GSM3215637 GSM3215637: scATAC-D0-29; Homo sapiens; ATAC-seq SRP151379 SRS3467390 GSM3215637 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215637 GSM3215637 GEO Accession GSM3215637 SRX4301991 GSM3215638 GSM3215638: scATAC-D0-2; Homo sapiens; ATAC-seq SRP151379 SRS3467394 GSM3215638 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215638 GSM3215638 GEO Accession GSM3215638 SRX4301992 GSM3215639 GSM3215639: scATAC-D0-30; Homo sapiens; ATAC-seq SRP151379 SRS3467389 GSM3215639 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215639 GSM3215639 GEO Accession GSM3215639 SRX4301993 GSM3215640 GSM3215640: scATAC-D0-31; Homo sapiens; ATAC-seq SRP151379 SRS3467399 GSM3215640 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215640 GSM3215640 GEO Accession GSM3215640 SRX4301994 GSM3215641 GSM3215641: scATAC-D0-32; Homo sapiens; ATAC-seq SRP151379 SRS3467397 GSM3215641 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215641 GSM3215641 GEO Accession GSM3215641 SRX4301995 GSM3215642 GSM3215642: scATAC-D0-33; Homo sapiens; ATAC-seq SRP151379 SRS3467483 GSM3215642 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215642 GSM3215642 GEO Accession GSM3215642 SRX4301996 GSM3215643 GSM3215643: scATAC-D0-34; Homo sapiens; ATAC-seq SRP151379 SRS3467398 GSM3215643 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215643 GSM3215643 GEO Accession GSM3215643 SRX4301997 GSM3215644 GSM3215644: scATAC-D0-35; Homo sapiens; ATAC-seq SRP151379 SRS3467445 GSM3215644 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215644 GSM3215644 GEO Accession GSM3215644 SRX4301998 GSM3215645 GSM3215645: scATAC-D0-36; Homo sapiens; ATAC-seq SRP151379 SRS3467393 GSM3215645 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215645 GSM3215645 GEO Accession GSM3215645 SRX4301999 GSM3215646 GSM3215646: scATAC-D0-37; Homo sapiens; ATAC-seq SRP151379 SRS3467396 GSM3215646 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215646 GSM3215646 GEO Accession GSM3215646 SRX4302000 GSM3215647 GSM3215647: scATAC-D0-38; Homo sapiens; ATAC-seq SRP151379 SRS3467391 GSM3215647 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215647 GSM3215647 GEO Accession GSM3215647 SRX4302001 GSM3215648 GSM3215648: scATAC-D0-39; Homo sapiens; ATAC-seq SRP151379 SRS3467395 GSM3215648 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215648 GSM3215648 GEO Accession GSM3215648 SRX4302002 GSM3215649 GSM3215649: scATAC-D0-3; Homo sapiens; ATAC-seq SRP151379 SRS3467406 GSM3215649 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215649 GSM3215649 GEO Accession GSM3215649 SRX4302003 GSM3215650 GSM3215650: scATAC-D0-40; Homo sapiens; ATAC-seq SRP151379 SRS3467401 GSM3215650 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215650 GSM3215650 GEO Accession GSM3215650 SRX4302004 GSM3215651 GSM3215651: scATAC-D0-41; Homo sapiens; ATAC-seq SRP151379 SRS3467400 GSM3215651 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215651 GSM3215651 GEO Accession GSM3215651 SRX4302005 GSM3215652 GSM3215652: scATAC-D0-42; Homo sapiens; ATAC-seq SRP151379 SRS3467403 GSM3215652 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215652 GSM3215652 GEO Accession GSM3215652 SRX4302006 GSM3215653 GSM3215653: scATAC-D0-43; Homo sapiens; ATAC-seq SRP151379 SRS3467408 GSM3215653 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215653 GSM3215653 GEO Accession GSM3215653 SRX4302007 GSM3215654 GSM3215654: scATAC-D0-44; Homo sapiens; ATAC-seq SRP151379 SRS3467407 GSM3215654 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215654 GSM3215654 GEO Accession GSM3215654 SRX4302008 GSM3215655 GSM3215655: scATAC-D0-45; Homo sapiens; ATAC-seq SRP151379 SRS3467402 GSM3215655 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215655 GSM3215655 GEO Accession GSM3215655 SRX4302009 GSM3215656 GSM3215656: scATAC-D0-46; Homo sapiens; ATAC-seq SRP151379 SRS3467405 GSM3215656 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215656 GSM3215656 GEO Accession GSM3215656 SRX4302010 GSM3215657 GSM3215657: scATAC-D0-47; Homo sapiens; ATAC-seq SRP151379 SRS3467404 GSM3215657 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215657 GSM3215657 GEO Accession GSM3215657 SRX4302011 GSM3215658 GSM3215658: scATAC-D0-48; Homo sapiens; ATAC-seq SRP151379 SRS3467410 GSM3215658 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215658 GSM3215658 GEO Accession GSM3215658 SRX4302012 GSM3215659 GSM3215659: scATAC-D0-49; Homo sapiens; ATAC-seq SRP151379 SRS3467412 GSM3215659 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215659 GSM3215659 GEO Accession GSM3215659 SRX4302013 GSM3215660 GSM3215660: scATAC-D0-4; Homo sapiens; ATAC-seq SRP151379 SRS3467409 GSM3215660 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215660 GSM3215660 GEO Accession GSM3215660 SRX4302014 GSM3215661 GSM3215661: scATAC-D0-50; Homo sapiens; ATAC-seq SRP151379 SRS3467411 GSM3215661 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215661 GSM3215661 GEO Accession GSM3215661 SRX4302015 GSM3215662 GSM3215662: scATAC-D0-51; Homo sapiens; ATAC-seq SRP151379 SRS3467419 GSM3215662 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215662 GSM3215662 GEO Accession GSM3215662 SRX4302016 GSM3215663 GSM3215663: scATAC-D0-52; Homo sapiens; ATAC-seq SRP151379 SRS3467413 GSM3215663 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215663 GSM3215663 GEO Accession GSM3215663 SRX4302017 GSM3215664 GSM3215664: scATAC-D0-53; Homo sapiens; ATAC-seq SRP151379 SRS3467415 GSM3215664 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215664 GSM3215664 GEO Accession GSM3215664 SRX4302018 GSM3215665 GSM3215665: scATAC-D0-54; Homo sapiens; ATAC-seq SRP151379 SRS3467475 GSM3215665 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215665 GSM3215665 GEO Accession GSM3215665 SRX4302019 GSM3215666 GSM3215666: scATAC-D0-55; Homo sapiens; ATAC-seq SRP151379 SRS3467416 GSM3215666 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215666 GSM3215666 GEO Accession GSM3215666 SRX4302020 GSM3215667 GSM3215667: scATAC-D0-56; Homo sapiens; ATAC-seq SRP151379 SRS3467421 GSM3215667 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215667 GSM3215667 GEO Accession GSM3215667 SRX4302021 GSM3215668 GSM3215668: scATAC-D0-57; Homo sapiens; ATAC-seq SRP151379 SRS3467414 GSM3215668 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215668 GSM3215668 GEO Accession GSM3215668 SRX4302022 GSM3215669 GSM3215669: scATAC-D0-58; Homo sapiens; ATAC-seq SRP151379 SRS3467417 GSM3215669 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215669 GSM3215669 GEO Accession GSM3215669 SRX4302023 GSM3215670 GSM3215670: scATAC-D0-59; Homo sapiens; ATAC-seq SRP151379 SRS3467423 GSM3215670 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215670 GSM3215670 GEO Accession GSM3215670 SRX4302024 GSM3215671 GSM3215671: scATAC-D0-5; Homo sapiens; ATAC-seq SRP151379 SRS3467422 GSM3215671 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215671 GSM3215671 GEO Accession GSM3215671 SRX4302025 GSM3215672 GSM3215672: scATAC-D0-60; Homo sapiens; ATAC-seq SRP151379 SRS3467420 GSM3215672 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215672 GSM3215672 GEO Accession GSM3215672 SRX4302026 GSM3215673 GSM3215673: scATAC-D0-61; Homo sapiens; ATAC-seq SRP151379 SRS3467418 GSM3215673 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215673 GSM3215673 GEO Accession GSM3215673 SRX4302027 GSM3215674 GSM3215674: scATAC-D0-62; Homo sapiens; ATAC-seq SRP151379 SRS3467482 GSM3215674 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215674 GSM3215674 GEO Accession GSM3215674 SRX4302028 GSM3215675 GSM3215675: scATAC-D0-63; Homo sapiens; ATAC-seq SRP151379 SRS3467448 GSM3215675 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215675 GSM3215675 GEO Accession GSM3215675 SRX4302029 GSM3215676 GSM3215676: scATAC-D0-64; Homo sapiens; ATAC-seq SRP151379 SRS3467427 GSM3215676 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215676 GSM3215676 GEO Accession GSM3215676 SRX4302030 GSM3215677 GSM3215677: scATAC-D0-65; Homo sapiens; ATAC-seq SRP151379 SRS3467425 GSM3215677 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215677 GSM3215677 GEO Accession GSM3215677 SRX4302031 GSM3215678 GSM3215678: scATAC-D0-66; Homo sapiens; ATAC-seq SRP151379 SRS3467429 GSM3215678 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215678 GSM3215678 GEO Accession GSM3215678 SRX4302032 GSM3215679 GSM3215679: scATAC-D0-67; Homo sapiens; ATAC-seq SRP151379 SRS3467436 GSM3215679 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215679 GSM3215679 GEO Accession GSM3215679 SRX4302033 GSM3215680 GSM3215680: scATAC-D0-68; Homo sapiens; ATAC-seq SRP151379 SRS3467426 GSM3215680 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215680 GSM3215680 GEO Accession GSM3215680 SRX4302034 GSM3215681 GSM3215681: scATAC-D0-69; Homo sapiens; ATAC-seq SRP151379 SRS3467432 GSM3215681 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215681 GSM3215681 GEO Accession GSM3215681 SRX4302035 GSM3215682 GSM3215682: scATAC-D0-6; Homo sapiens; ATAC-seq SRP151379 SRS3467424 GSM3215682 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215682 GSM3215682 GEO Accession GSM3215682 SRX4302036 GSM3215683 GSM3215683: scATAC-D0-70; Homo sapiens; ATAC-seq SRP151379 SRS3467430 GSM3215683 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215683 GSM3215683 GEO Accession GSM3215683 SRX4302037 GSM3215684 GSM3215684: scATAC-D0-71; Homo sapiens; ATAC-seq SRP151379 SRS3467428 GSM3215684 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215684 GSM3215684 GEO Accession GSM3215684 SRX4302038 GSM3215685 GSM3215685: scATAC-D0-72; Homo sapiens; ATAC-seq SRP151379 SRS3467431 GSM3215685 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215685 GSM3215685 GEO Accession GSM3215685 SRX4302039 GSM3215686 GSM3215686: scATAC-D0-73; Homo sapiens; ATAC-seq SRP151379 SRS3467434 GSM3215686 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215686 GSM3215686 GEO Accession GSM3215686 SRX4302040 GSM3215687 GSM3215687: scATAC-D0-74; Homo sapiens; ATAC-seq SRP151379 SRS3467433 GSM3215687 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215687 GSM3215687 GEO Accession GSM3215687 SRX4302041 GSM3215688 GSM3215688: scATAC-D0-75; Homo sapiens; ATAC-seq SRP151379 SRS3467527 GSM3215688 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215688 GSM3215688 GEO Accession GSM3215688 SRX4302042 GSM3215689 GSM3215689: scATAC-D0-76; Homo sapiens; ATAC-seq SRP151379 SRS3467528 GSM3215689 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215689 GSM3215689 GEO Accession GSM3215689 SRX4302043 GSM3215690 GSM3215690: scATAC-D0-77; Homo sapiens; ATAC-seq SRP151379 SRS3467484 GSM3215690 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215690 GSM3215690 GEO Accession GSM3215690 SRX4302044 GSM3215691 GSM3215691: scATAC-D0-78; Homo sapiens; ATAC-seq SRP151379 SRS3467438 GSM3215691 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215691 GSM3215691 GEO Accession GSM3215691 SRX4302045 GSM3215692 GSM3215692: scATAC-D0-79; Homo sapiens; ATAC-seq SRP151379 SRS3467437 GSM3215692 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215692 GSM3215692 GEO Accession GSM3215692 SRX4302046 GSM3215693 GSM3215693: scATAC-D0-7; Homo sapiens; ATAC-seq SRP151379 SRS3467435 GSM3215693 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215693 GSM3215693 GEO Accession GSM3215693 SRX4302047 GSM3215694 GSM3215694: scATAC-D0-80; Homo sapiens; ATAC-seq SRP151379 SRS3467440 GSM3215694 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215694 GSM3215694 GEO Accession GSM3215694 SRX4302048 GSM3215695 GSM3215695: scATAC-D0-81; Homo sapiens; ATAC-seq SRP151379 SRS3467529 GSM3215695 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215695 GSM3215695 GEO Accession GSM3215695 SRX4302049 GSM3215696 GSM3215696: scATAC-D0-82; Homo sapiens; ATAC-seq SRP151379 SRS3467444 GSM3215696 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215696 GSM3215696 GEO Accession GSM3215696 SRX4302050 GSM3215697 GSM3215697: scATAC-D0-83; Homo sapiens; ATAC-seq SRP151379 SRS3467442 GSM3215697 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215697 GSM3215697 GEO Accession GSM3215697 SRX4302051 GSM3215698 GSM3215698: scATAC-D0-84; Homo sapiens; ATAC-seq SRP151379 SRS3467446 GSM3215698 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215698 GSM3215698 GEO Accession GSM3215698 SRX4302052 GSM3215699 GSM3215699: scATAC-D0-85; Homo sapiens; ATAC-seq SRP151379 SRS3467450 GSM3215699 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215699 GSM3215699 GEO Accession GSM3215699 SRX4302053 GSM3215700 GSM3215700: scATAC-D0-86; Homo sapiens; ATAC-seq SRP151379 SRS3467495 GSM3215700 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215700 GSM3215700 GEO Accession GSM3215700 SRX4302054 GSM3215701 GSM3215701: scATAC-D0-87; Homo sapiens; ATAC-seq SRP151379 SRS3467447 GSM3215701 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215701 GSM3215701 GEO Accession GSM3215701 SRX4302055 GSM3215702 GSM3215702: scATAC-D0-88; Homo sapiens; ATAC-seq SRP151379 SRS3467451 GSM3215702 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215702 GSM3215702 GEO Accession GSM3215702 SRX4302056 GSM3215703 GSM3215703: scATAC-D0-89; Homo sapiens; ATAC-seq SRP151379 SRS3467452 GSM3215703 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215703 GSM3215703 GEO Accession GSM3215703 SRX4302057 GSM3215704 GSM3215704: scATAC-D0-8; Homo sapiens; ATAC-seq SRP151379 SRS3467487 GSM3215704 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215704 GSM3215704 GEO Accession GSM3215704 SRX4302058 GSM3215705 GSM3215705: scATAC-D0-90; Homo sapiens; ATAC-seq SRP151379 SRS3467449 GSM3215705 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215705 GSM3215705 GEO Accession GSM3215705 SRX4302059 GSM3215706 GSM3215706: scATAC-D0-91; Homo sapiens; ATAC-seq SRP151379 SRS3467453 GSM3215706 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215706 GSM3215706 GEO Accession GSM3215706 SRX4302060 GSM3215707 GSM3215707: scATAC-D0-92; Homo sapiens; ATAC-seq SRP151379 SRS3467489 GSM3215707 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215707 GSM3215707 GEO Accession GSM3215707 SRX4302061 GSM3215708 GSM3215708: scATAC-D0-93; Homo sapiens; ATAC-seq SRP151379 SRS3467455 GSM3215708 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215708 GSM3215708 GEO Accession GSM3215708 SRX4302062 GSM3215709 GSM3215709: scATAC-D0-94; Homo sapiens; ATAC-seq SRP151379 SRS3467593 GSM3215709 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215709 GSM3215709 GEO Accession GSM3215709 SRX4302063 GSM3215710 GSM3215710: scATAC-D0-95; Homo sapiens; ATAC-seq SRP151379 SRS3467458 GSM3215710 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215710 GSM3215710 GEO Accession GSM3215710 SRX4302064 GSM3215711 GSM3215711: scATAC-D0-96; Homo sapiens; ATAC-seq SRP151379 SRS3467516 GSM3215711 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215711 GSM3215711 GEO Accession GSM3215711 SRX4302065 GSM3215712 GSM3215712: scATAC-D0-9; Homo sapiens; ATAC-seq SRP151379 SRS3467457 GSM3215712 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215712 GSM3215712 GEO Accession GSM3215712 SRX4302066 GSM3215713 GSM3215713: scATAC-D3-10; Homo sapiens; ATAC-seq SRP151379 SRS3467456 GSM3215713 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215713 GSM3215713 GEO Accession GSM3215713 SRX4302067 GSM3215714 GSM3215714: scATAC-D3-11; Homo sapiens; ATAC-seq SRP151379 SRS3467462 GSM3215714 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215714 GSM3215714 GEO Accession GSM3215714 SRX4302068 GSM3215715 GSM3215715: scATAC-D3-12; Homo sapiens; ATAC-seq SRP151379 SRS3467459 GSM3215715 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215715 GSM3215715 GEO Accession GSM3215715 SRX4302069 GSM3215716 GSM3215716: scATAC-D3-13; Homo sapiens; ATAC-seq SRP151379 SRS3467460 GSM3215716 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215716 GSM3215716 GEO Accession GSM3215716 SRX4302070 GSM3215717 GSM3215717: scATAC-D3-14; Homo sapiens; ATAC-seq SRP151379 SRS3467461 GSM3215717 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215717 GSM3215717 GEO Accession GSM3215717 SRX4302071 GSM3215718 GSM3215718: scATAC-D3-15; Homo sapiens; ATAC-seq SRP151379 SRS3467525 GSM3215718 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215718 GSM3215718 GEO Accession GSM3215718 SRX4302072 GSM3215719 GSM3215719: scATAC-D3-16; Homo sapiens; ATAC-seq SRP151379 SRS3467463 GSM3215719 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215719 GSM3215719 GEO Accession GSM3215719 SRX4302073 GSM3215720 GSM3215720: scATAC-D3-17; Homo sapiens; ATAC-seq SRP151379 SRS3467509 GSM3215720 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215720 GSM3215720 GEO Accession GSM3215720 SRX4302074 GSM3215721 GSM3215721: scATAC-D3-18; Homo sapiens; ATAC-seq SRP151379 SRS3467464 GSM3215721 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215721 GSM3215721 GEO Accession GSM3215721 SRX4302075 GSM3215722 GSM3215722: scATAC-D3-19; Homo sapiens; ATAC-seq SRP151379 SRS3467514 GSM3215722 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215722 GSM3215722 GEO Accession GSM3215722 SRX4302076 GSM3215723 GSM3215723: scATAC-D3-1; Homo sapiens; ATAC-seq SRP151379 SRS3467469 GSM3215723 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215723 GSM3215723 GEO Accession GSM3215723 SRX4302077 GSM3215724 GSM3215724: scATAC-D3-20; Homo sapiens; ATAC-seq SRP151379 SRS3467467 GSM3215724 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215724 GSM3215724 GEO Accession GSM3215724 SRX4302078 GSM3215725 GSM3215725: scATAC-D3-21; Homo sapiens; ATAC-seq SRP151379 SRS3467468 GSM3215725 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215725 GSM3215725 GEO Accession GSM3215725 SRX4302079 GSM3215726 GSM3215726: scATAC-D3-22; Homo sapiens; ATAC-seq SRP151379 SRS3467472 GSM3215726 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215726 GSM3215726 GEO Accession GSM3215726 SRX4302080 GSM3215727 GSM3215727: scATAC-D3-23; Homo sapiens; ATAC-seq SRP151379 SRS3467471 GSM3215727 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215727 GSM3215727 GEO Accession GSM3215727 SRX4302081 GSM3215728 GSM3215728: scATAC-D3-24; Homo sapiens; ATAC-seq SRP151379 SRS3467524 GSM3215728 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215728 GSM3215728 GEO Accession GSM3215728 SRX4302082 GSM3215729 GSM3215729: scATAC-D3-25; Homo sapiens; ATAC-seq SRP151379 SRS3467470 GSM3215729 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215729 GSM3215729 GEO Accession GSM3215729 SRX4302083 GSM3215730 GSM3215730: scATAC-D3-26; Homo sapiens; ATAC-seq SRP151379 SRS3467473 GSM3215730 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215730 GSM3215730 GEO Accession GSM3215730 SRX4302084 GSM3215731 GSM3215731: scATAC-D3-27; Homo sapiens; ATAC-seq SRP151379 SRS3467474 GSM3215731 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215731 GSM3215731 GEO Accession GSM3215731 SRX4302085 GSM3215732 GSM3215732: scATAC-D3-28; Homo sapiens; ATAC-seq SRP151379 SRS3467476 GSM3215732 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215732 GSM3215732 GEO Accession GSM3215732 SRX4302086 GSM3215733 GSM3215733: scATAC-D3-29; Homo sapiens; ATAC-seq SRP151379 SRS3467477 GSM3215733 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215733 GSM3215733 GEO Accession GSM3215733 SRX4302087 GSM3215734 GSM3215734: scATAC-D3-2; Homo sapiens; ATAC-seq SRP151379 SRS3467478 GSM3215734 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215734 GSM3215734 GEO Accession GSM3215734 SRX4302088 GSM3215735 GSM3215735: scATAC-D3-30; Homo sapiens; ATAC-seq SRP151379 SRS3467480 GSM3215735 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215735 GSM3215735 GEO Accession GSM3215735 SRX4302089 GSM3215736 GSM3215736: scATAC-D3-31; Homo sapiens; ATAC-seq SRP151379 SRS3467481 GSM3215736 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215736 GSM3215736 GEO Accession GSM3215736 SRX4302090 GSM3215737 GSM3215737: scATAC-D3-32; Homo sapiens; ATAC-seq SRP151379 SRS3467594 GSM3215737 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215737 GSM3215737 GEO Accession GSM3215737 SRX4302091 GSM3215738 GSM3215738: scATAC-D3-33; Homo sapiens; ATAC-seq SRP151379 SRS3467485 GSM3215738 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215738 GSM3215738 GEO Accession GSM3215738 SRX4302092 GSM3215739 GSM3215739: scATAC-D3-34; Homo sapiens; ATAC-seq SRP151379 SRS3467545 GSM3215739 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215739 GSM3215739 GEO Accession GSM3215739 SRX4302093 GSM3215740 GSM3215740: scATAC-D3-35; Homo sapiens; ATAC-seq SRP151379 SRS3467479 GSM3215740 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215740 GSM3215740 GEO Accession GSM3215740 SRX4302094 GSM3215741 GSM3215741: scATAC-D3-36; Homo sapiens; ATAC-seq SRP151379 SRS3467526 GSM3215741 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215741 GSM3215741 GEO Accession GSM3215741 SRX4302095 GSM3215742 GSM3215742: scATAC-D3-37; Homo sapiens; ATAC-seq SRP151379 SRS3466219 GSM3215742 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215742 GSM3215742 GEO Accession GSM3215742 SRX4302096 GSM3215743 GSM3215743: scATAC-D3-38; Homo sapiens; ATAC-seq SRP151379 SRS3466218 GSM3215743 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215743 GSM3215743 GEO Accession GSM3215743 SRX4302097 GSM3215744 GSM3215744: scATAC-D3-39; Homo sapiens; ATAC-seq SRP151379 SRS3466220 GSM3215744 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215744 GSM3215744 GEO Accession GSM3215744 SRX4302098 GSM3215745 GSM3215745: scATAC-D3-3; Homo sapiens; ATAC-seq SRP151379 SRS3466221 GSM3215745 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215745 GSM3215745 GEO Accession GSM3215745 SRX4302099 GSM3215746 GSM3215746: scATAC-D3-40; Homo sapiens; ATAC-seq SRP151379 SRS3466223 GSM3215746 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215746 GSM3215746 GEO Accession GSM3215746 SRX4302100 GSM3215747 GSM3215747: scATAC-D3-41; Homo sapiens; ATAC-seq SRP151379 SRS3466278 GSM3215747 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215747 GSM3215747 GEO Accession GSM3215747 SRX4302101 GSM3215748 GSM3215748: scATAC-D3-42; Homo sapiens; ATAC-seq SRP151379 SRS3466224 GSM3215748 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215748 GSM3215748 GEO Accession GSM3215748 SRX4302102 GSM3215749 GSM3215749: scATAC-D3-43; Homo sapiens; ATAC-seq SRP151379 SRS3466222 GSM3215749 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215749 GSM3215749 GEO Accession GSM3215749 SRX4302103 GSM3215750 GSM3215750: scATAC-D3-44; Homo sapiens; ATAC-seq SRP151379 SRS3466225 GSM3215750 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215750 GSM3215750 GEO Accession GSM3215750 SRX4302104 GSM3215751 GSM3215751: scATAC-D3-45; Homo sapiens; ATAC-seq SRP151379 SRS3466227 GSM3215751 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215751 GSM3215751 GEO Accession GSM3215751 SRX4302105 GSM3215752 GSM3215752: scATAC-D3-46; Homo sapiens; ATAC-seq SRP151379 SRS3466226 GSM3215752 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215752 GSM3215752 GEO Accession GSM3215752 SRX4302106 GSM3215753 GSM3215753: scATAC-D3-47; Homo sapiens; ATAC-seq SRP151379 SRS3466228 GSM3215753 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215753 GSM3215753 GEO Accession GSM3215753 SRX4302107 GSM3215754 GSM3215754: scATAC-D3-48; Homo sapiens; ATAC-seq SRP151379 SRS3466229 GSM3215754 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215754 GSM3215754 GEO Accession GSM3215754 SRX4302108 GSM3215755 GSM3215755: scATAC-D3-49; Homo sapiens; ATAC-seq SRP151379 SRS3466232 GSM3215755 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215755 GSM3215755 GEO Accession GSM3215755 SRX4302109 GSM3215756 GSM3215756: scATAC-D3-4; Homo sapiens; ATAC-seq SRP151379 SRS3466230 GSM3215756 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215756 GSM3215756 GEO Accession GSM3215756 SRX4302110 GSM3215757 GSM3215757: scATAC-D3-50; Homo sapiens; ATAC-seq SRP151379 SRS3466231 GSM3215757 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215757 GSM3215757 GEO Accession GSM3215757 SRX4302111 GSM3215758 GSM3215758: scATAC-D3-51; Homo sapiens; ATAC-seq SRP151379 SRS3466234 GSM3215758 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215758 GSM3215758 GEO Accession GSM3215758 SRX4302112 GSM3215759 GSM3215759: scATAC-D3-52; Homo sapiens; ATAC-seq SRP151379 SRS3466235 GSM3215759 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215759 GSM3215759 GEO Accession GSM3215759 SRX4302113 GSM3215760 GSM3215760: scATAC-D3-53; Homo sapiens; ATAC-seq SRP151379 SRS3466238 GSM3215760 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215760 GSM3215760 GEO Accession GSM3215760 SRX4302114 GSM3215761 GSM3215761: scATAC-D3-54; Homo sapiens; ATAC-seq SRP151379 SRS3466233 GSM3215761 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215761 GSM3215761 GEO Accession GSM3215761 SRX4302115 GSM3215762 GSM3215762: scATAC-D3-55; Homo sapiens; ATAC-seq SRP151379 SRS3466236 GSM3215762 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215762 GSM3215762 GEO Accession GSM3215762 SRX4302116 GSM3215763 GSM3215763: scATAC-D3-56; Homo sapiens; ATAC-seq SRP151379 SRS3466240 GSM3215763 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215763 GSM3215763 GEO Accession GSM3215763 SRX4302117 GSM3215764 GSM3215764: scATAC-D3-57; Homo sapiens; ATAC-seq SRP151379 SRS3466239 GSM3215764 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215764 GSM3215764 GEO Accession GSM3215764 SRX4302118 GSM3215765 GSM3215765: scATAC-D3-58; Homo sapiens; ATAC-seq SRP151379 SRS3466237 GSM3215765 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215765 GSM3215765 GEO Accession GSM3215765 SRX4302119 GSM3215766 GSM3215766: scATAC-D3-59; Homo sapiens; ATAC-seq SRP151379 SRS3466241 GSM3215766 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215766 GSM3215766 GEO Accession GSM3215766 SRX4302120 GSM3215767 GSM3215767: scATAC-D3-5; Homo sapiens; ATAC-seq SRP151379 SRS3466265 GSM3215767 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215767 GSM3215767 GEO Accession GSM3215767 SRX4302121 GSM3215768 GSM3215768: scATAC-D3-60; Homo sapiens; ATAC-seq SRP151379 SRS3466242 GSM3215768 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215768 GSM3215768 GEO Accession GSM3215768 SRX4302122 GSM3215769 GSM3215769: scATAC-D3-61; Homo sapiens; ATAC-seq SRP151379 SRS3466243 GSM3215769 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215769 GSM3215769 GEO Accession GSM3215769 SRX4302123 GSM3215770 GSM3215770: scATAC-D3-62; Homo sapiens; ATAC-seq SRP151379 SRS3466244 GSM3215770 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215770 GSM3215770 GEO Accession GSM3215770 SRX4302124 GSM3215771 GSM3215771: scATAC-D3-63; Homo sapiens; ATAC-seq SRP151379 SRS3466245 GSM3215771 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215771 GSM3215771 GEO Accession GSM3215771 SRX4302125 GSM3215772 GSM3215772: scATAC-D3-64; Homo sapiens; ATAC-seq SRP151379 SRS3467488 GSM3215772 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215772 GSM3215772 GEO Accession GSM3215772 SRX4302126 GSM3215773 GSM3215773: scATAC-D3-65; Homo sapiens; ATAC-seq SRP151379 SRS3467490 GSM3215773 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215773 GSM3215773 GEO Accession GSM3215773 SRX4302127 GSM3215774 GSM3215774: scATAC-D3-66; Homo sapiens; ATAC-seq SRP151379 SRS3467492 GSM3215774 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215774 GSM3215774 GEO Accession GSM3215774 SRX4302128 GSM3215775 GSM3215775: scATAC-D3-67; Homo sapiens; ATAC-seq SRP151379 SRS3467491 GSM3215775 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215775 GSM3215775 GEO Accession GSM3215775 SRX4302129 GSM3215776 GSM3215776: scATAC-D3-68; Homo sapiens; ATAC-seq SRP151379 SRS3467496 GSM3215776 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215776 GSM3215776 GEO Accession GSM3215776 SRX4302130 GSM3215777 GSM3215777: scATAC-D3-69; Homo sapiens; ATAC-seq SRP151379 SRS3467493 GSM3215777 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215777 GSM3215777 GEO Accession GSM3215777 SRX4302131 GSM3215778 GSM3215778: scATAC-D3-6; Homo sapiens; ATAC-seq SRP151379 SRS3467497 GSM3215778 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215778 GSM3215778 GEO Accession GSM3215778 SRX4302132 GSM3215779 GSM3215779: scATAC-D3-70; Homo sapiens; ATAC-seq SRP151379 SRS3467499 GSM3215779 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215779 GSM3215779 GEO Accession GSM3215779 SRX4302133 GSM3215780 GSM3215780: scATAC-D3-71; Homo sapiens; ATAC-seq SRP151379 SRS3467498 GSM3215780 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215780 GSM3215780 GEO Accession GSM3215780 SRX4302134 GSM3215781 GSM3215781: scATAC-D3-72; Homo sapiens; ATAC-seq SRP151379 SRS3467494 GSM3215781 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215781 GSM3215781 GEO Accession GSM3215781 SRX4302135 GSM3215782 GSM3215782: scATAC-D3-73; Homo sapiens; ATAC-seq SRP151379 SRS3467500 GSM3215782 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215782 GSM3215782 GEO Accession GSM3215782 SRX4302136 GSM3215783 GSM3215783: scATAC-D3-74; Homo sapiens; ATAC-seq SRP151379 SRS3467501 GSM3215783 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215783 GSM3215783 GEO Accession GSM3215783 SRX4302137 GSM3215784 GSM3215784: scATAC-D3-75; Homo sapiens; ATAC-seq SRP151379 SRS3467502 GSM3215784 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215784 GSM3215784 GEO Accession GSM3215784 SRX4302138 GSM3215785 GSM3215785: scATAC-D3-76; Homo sapiens; ATAC-seq SRP151379 SRS3467503 GSM3215785 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215785 GSM3215785 GEO Accession GSM3215785 SRX4302139 GSM3215786 GSM3215786: scATAC-D3-77; Homo sapiens; ATAC-seq SRP151379 SRS3467507 GSM3215786 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215786 GSM3215786 GEO Accession GSM3215786 SRX4302140 GSM3215787 GSM3215787: scATAC-D3-78; Homo sapiens; ATAC-seq SRP151379 SRS3467504 GSM3215787 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215787 GSM3215787 GEO Accession GSM3215787 SRX4302141 GSM3215788 GSM3215788: scATAC-D3-79; Homo sapiens; ATAC-seq SRP151379 SRS3467510 GSM3215788 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215788 GSM3215788 GEO Accession GSM3215788 SRX4302142 GSM3215789 GSM3215789: scATAC-D3-7; Homo sapiens; ATAC-seq SRP151379 SRS3467505 GSM3215789 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215789 GSM3215789 GEO Accession GSM3215789 SRX4302143 GSM3215790 GSM3215790: scATAC-D3-80; Homo sapiens; ATAC-seq SRP151379 SRS3467506 GSM3215790 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215790 GSM3215790 GEO Accession GSM3215790 SRX4302144 GSM3215791 GSM3215791: scATAC-D3-81; Homo sapiens; ATAC-seq SRP151379 SRS3467512 GSM3215791 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215791 GSM3215791 GEO Accession GSM3215791 SRX4302145 GSM3215792 GSM3215792: scATAC-D3-82; Homo sapiens; ATAC-seq SRP151379 SRS3467513 GSM3215792 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215792 GSM3215792 GEO Accession GSM3215792 SRX4302146 GSM3215793 GSM3215793: scATAC-D3-83; Homo sapiens; ATAC-seq SRP151379 SRS3467511 GSM3215793 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215793 GSM3215793 GEO Accession GSM3215793 SRX4302147 GSM3215794 GSM3215794: scATAC-D3-84; Homo sapiens; ATAC-seq SRP151379 SRS3467518 GSM3215794 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215794 GSM3215794 GEO Accession GSM3215794 SRX4302148 GSM3215795 GSM3215795: scATAC-D3-85; Homo sapiens; ATAC-seq SRP151379 SRS3467515 GSM3215795 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215795 GSM3215795 GEO Accession GSM3215795 SRX4302149 GSM3215796 GSM3215796: scATAC-D3-86; Homo sapiens; ATAC-seq SRP151379 SRS3467517 GSM3215796 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215796 GSM3215796 GEO Accession GSM3215796 SRX4302150 GSM3215797 GSM3215797: scATAC-D3-87; Homo sapiens; ATAC-seq SRP151379 SRS3467519 GSM3215797 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215797 GSM3215797 GEO Accession GSM3215797 SRX4302151 GSM3215798 GSM3215798: scATAC-D3-88; Homo sapiens; ATAC-seq SRP151379 SRS3467521 GSM3215798 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215798 GSM3215798 GEO Accession GSM3215798 SRX4302152 GSM3215799 GSM3215799: scATAC-D3-89; Homo sapiens; ATAC-seq SRP151379 SRS3467522 GSM3215799 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215799 GSM3215799 GEO Accession GSM3215799 SRX4302153 GSM3215800 GSM3215800: scATAC-D3-8; Homo sapiens; ATAC-seq SRP151379 SRS3467520 GSM3215800 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215800 GSM3215800 GEO Accession GSM3215800 SRX4302154 GSM3215801 GSM3215801: scATAC-D3-90; Homo sapiens; ATAC-seq SRP151379 SRS3467523 GSM3215801 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215801 GSM3215801 GEO Accession GSM3215801 SRX4302155 GSM3215802 GSM3215802: scATAC-D3-91; Homo sapiens; ATAC-seq SRP151379 SRS3466251 GSM3215802 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215802 GSM3215802 GEO Accession GSM3215802 SRX4302156 GSM3215803 GSM3215803: scATAC-D3-92; Homo sapiens; ATAC-seq SRP151379 SRS3466246 GSM3215803 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215803 GSM3215803 GEO Accession GSM3215803 SRX4302157 GSM3215804 GSM3215804: scATAC-D3-93; Homo sapiens; ATAC-seq SRP151379 SRS3466247 GSM3215804 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215804 GSM3215804 GEO Accession GSM3215804 SRX4302158 GSM3215805 GSM3215805: scATAC-D3-94; Homo sapiens; ATAC-seq SRP151379 SRS3466248 GSM3215805 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215805 GSM3215805 GEO Accession GSM3215805 SRX4302159 GSM3215806 GSM3215806: scATAC-D3-95; Homo sapiens; ATAC-seq SRP151379 SRS3466249 GSM3215806 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215806 GSM3215806 GEO Accession GSM3215806 SRX4302160 GSM3215807 GSM3215807: scATAC-D3-96; Homo sapiens; ATAC-seq SRP151379 SRS3466320 GSM3215807 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215807 GSM3215807 GEO Accession GSM3215807 SRX4302161 GSM3215808 GSM3215808: scATAC-D3-9; Homo sapiens; ATAC-seq SRP151379 SRS3466250 GSM3215808 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215808 GSM3215808 GEO Accession GSM3215808 SRX4302162 GSM3215809 GSM3215809: scATAC-D6-10; Homo sapiens; ATAC-seq SRP151379 SRS3466252 GSM3215809 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215809 GSM3215809 GEO Accession GSM3215809 SRX4302163 GSM3215810 GSM3215810: scATAC-D6-11; Homo sapiens; ATAC-seq SRP151379 SRS3466255 GSM3215810 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215810 GSM3215810 GEO Accession GSM3215810 SRX4302164 GSM3215811 GSM3215811: scATAC-D6-12; Homo sapiens; ATAC-seq SRP151379 SRS3466398 GSM3215811 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215811 GSM3215811 GEO Accession GSM3215811 SRX4302165 GSM3215812 GSM3215812: scATAC-D6-13; Homo sapiens; ATAC-seq SRP151379 SRS3466253 GSM3215812 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215812 GSM3215812 GEO Accession GSM3215812 SRX4302166 GSM3215813 GSM3215813: scATAC-D6-14; Homo sapiens; ATAC-seq SRP151379 SRS3466254 GSM3215813 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215813 GSM3215813 GEO Accession GSM3215813 SRX4302167 GSM3215814 GSM3215814: scATAC-D6-15; Homo sapiens; ATAC-seq SRP151379 SRS3466257 GSM3215814 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215814 GSM3215814 GEO Accession GSM3215814 SRX4302168 GSM3215815 GSM3215815: scATAC-D6-16; Homo sapiens; ATAC-seq SRP151379 SRS3466261 GSM3215815 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215815 GSM3215815 GEO Accession GSM3215815 SRX4302169 GSM3215816 GSM3215816: scATAC-D6-17; Homo sapiens; ATAC-seq SRP151379 SRS3466256 GSM3215816 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215816 GSM3215816 GEO Accession GSM3215816 SRX4302170 GSM3215817 GSM3215817: scATAC-D6-18; Homo sapiens; ATAC-seq SRP151379 SRS3466258 GSM3215817 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215817 GSM3215817 GEO Accession GSM3215817 SRX4302171 GSM3215818 GSM3215818: scATAC-D6-19; Homo sapiens; ATAC-seq SRP151379 SRS3466260 GSM3215818 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215818 GSM3215818 GEO Accession GSM3215818 SRX4302172 GSM3215819 GSM3215819: scATAC-D6-1; Homo sapiens; ATAC-seq SRP151379 SRS3466268 GSM3215819 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215819 GSM3215819 GEO Accession GSM3215819 SRX4302173 GSM3215820 GSM3215820: scATAC-D6-20; Homo sapiens; ATAC-seq SRP151379 SRS3466262 GSM3215820 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215820 GSM3215820 GEO Accession GSM3215820 SRX4302174 GSM3215821 GSM3215821: scATAC-D6-21; Homo sapiens; ATAC-seq SRP151379 SRS3466259 GSM3215821 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215821 GSM3215821 GEO Accession GSM3215821 SRX4302175 GSM3215822 GSM3215822: scATAC-D6-22; Homo sapiens; ATAC-seq SRP151379 SRS3466264 GSM3215822 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215822 GSM3215822 GEO Accession GSM3215822 SRX4302176 GSM3215823 GSM3215823: scATAC-D6-23; Homo sapiens; ATAC-seq SRP151379 SRS3466263 GSM3215823 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215823 GSM3215823 GEO Accession GSM3215823 SRX4302177 GSM3215824 GSM3215824: scATAC-D6-24; Homo sapiens; ATAC-seq SRP151379 SRS3466266 GSM3215824 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215824 GSM3215824 GEO Accession GSM3215824 SRX4302178 GSM3215825 GSM3215825: scATAC-D6-25; Homo sapiens; ATAC-seq SRP151379 SRS3466267 GSM3215825 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215825 GSM3215825 GEO Accession GSM3215825 SRX4302179 GSM3215826 GSM3215826: scATAC-D6-26; Homo sapiens; ATAC-seq SRP151379 SRS3466269 GSM3215826 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215826 GSM3215826 GEO Accession GSM3215826 SRX4302180 GSM3215827 GSM3215827: scATAC-D6-27; Homo sapiens; ATAC-seq SRP151379 SRS3466270 GSM3215827 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215827 GSM3215827 GEO Accession GSM3215827 SRX4302181 GSM3215828 GSM3215828: scATAC-D6-28; Homo sapiens; ATAC-seq SRP151379 SRS3466272 GSM3215828 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215828 GSM3215828 GEO Accession GSM3215828 SRX4302182 GSM3215829 GSM3215829: scATAC-D6-29; Homo sapiens; ATAC-seq SRP151379 SRS3466276 GSM3215829 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215829 GSM3215829 GEO Accession GSM3215829 SRX4302183 GSM3215830 GSM3215830: scATAC-D6-2; Homo sapiens; ATAC-seq SRP151379 SRS3466271 GSM3215830 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215830 GSM3215830 GEO Accession GSM3215830 SRX4302184 GSM3215831 GSM3215831: scATAC-D6-30; Homo sapiens; ATAC-seq SRP151379 SRS3466274 GSM3215831 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215831 GSM3215831 GEO Accession GSM3215831 SRX4302185 GSM3215832 GSM3215832: scATAC-D6-31; Homo sapiens; ATAC-seq SRP151379 SRS3466365 GSM3215832 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215832 GSM3215832 GEO Accession GSM3215832 SRX4302186 GSM3215833 GSM3215833: scATAC-D6-32; Homo sapiens; ATAC-seq SRP151379 SRS3466273 GSM3215833 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215833 GSM3215833 GEO Accession GSM3215833 SRX4302187 GSM3215834 GSM3215834: scATAC-D6-33; Homo sapiens; ATAC-seq SRP151379 SRS3466275 GSM3215834 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215834 GSM3215834 GEO Accession GSM3215834 SRX4302188 GSM3215835 GSM3215835: scATAC-D6-34; Homo sapiens; ATAC-seq SRP151379 SRS3466279 GSM3215835 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215835 GSM3215835 GEO Accession GSM3215835 SRX4302189 GSM3215836 GSM3215836: scATAC-D6-35; Homo sapiens; ATAC-seq SRP151379 SRS3466281 GSM3215836 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215836 GSM3215836 GEO Accession GSM3215836 SRX4302190 GSM3215837 GSM3215837: scATAC-D6-36; Homo sapiens; ATAC-seq SRP151379 SRS3466277 GSM3215837 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215837 GSM3215837 GEO Accession GSM3215837 SRX4302191 GSM3215838 GSM3215838: scATAC-D6-37; Homo sapiens; ATAC-seq SRP151379 SRS3466280 GSM3215838 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215838 GSM3215838 GEO Accession GSM3215838 SRX4302192 GSM3215839 GSM3215839: scATAC-D6-38; Homo sapiens; ATAC-seq SRP151379 SRS3467535 GSM3215839 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215839 GSM3215839 GEO Accession GSM3215839 SRX4302193 GSM3215840 GSM3215840: scATAC-D6-39; Homo sapiens; ATAC-seq SRP151379 SRS3467530 GSM3215840 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215840 GSM3215840 GEO Accession GSM3215840 SRX4302194 GSM3215841 GSM3215841: scATAC-D6-3; Homo sapiens; ATAC-seq SRP151379 SRS3467532 GSM3215841 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215841 GSM3215841 GEO Accession GSM3215841 SRX4302195 GSM3215842 GSM3215842: scATAC-D6-40; Homo sapiens; ATAC-seq SRP151379 SRS3467531 GSM3215842 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215842 GSM3215842 GEO Accession GSM3215842 SRX4302196 GSM3215843 GSM3215843: scATAC-D6-41; Homo sapiens; ATAC-seq SRP151379 SRS3467539 GSM3215843 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215843 GSM3215843 GEO Accession GSM3215843 SRX4302197 GSM3215844 GSM3215844: scATAC-D6-42; Homo sapiens; ATAC-seq SRP151379 SRS3467538 GSM3215844 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215844 GSM3215844 GEO Accession GSM3215844 SRX4302198 GSM3215845 GSM3215845: scATAC-D6-43; Homo sapiens; ATAC-seq SRP151379 SRS3467536 GSM3215845 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215845 GSM3215845 GEO Accession GSM3215845 SRX4302199 GSM3215846 GSM3215846: scATAC-D6-44; Homo sapiens; ATAC-seq SRP151379 SRS3467543 GSM3215846 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215846 GSM3215846 GEO Accession GSM3215846 SRX4302200 GSM3215847 GSM3215847: scATAC-D6-45; Homo sapiens; ATAC-seq SRP151379 SRS3467533 GSM3215847 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215847 GSM3215847 GEO Accession GSM3215847 SRX4302201 GSM3215848 GSM3215848: scATAC-D6-46; Homo sapiens; ATAC-seq SRP151379 SRS3467534 GSM3215848 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215848 GSM3215848 GEO Accession GSM3215848 SRX4302202 GSM3215849 GSM3215849: scATAC-D6-47; Homo sapiens; ATAC-seq SRP151379 SRS3467537 GSM3215849 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215849 GSM3215849 GEO Accession GSM3215849 SRX4302203 GSM3215850 GSM3215850: scATAC-D6-48; Homo sapiens; ATAC-seq SRP151379 SRS3467542 GSM3215850 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215850 GSM3215850 GEO Accession GSM3215850 SRX4302204 GSM3215851 GSM3215851: scATAC-D6-49; Homo sapiens; ATAC-seq SRP151379 SRS3467544 GSM3215851 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215851 GSM3215851 GEO Accession GSM3215851 SRX4302205 GSM3215852 GSM3215852: scATAC-D6-4; Homo sapiens; ATAC-seq SRP151379 SRS3467540 GSM3215852 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215852 GSM3215852 GEO Accession GSM3215852 SRX4302206 GSM3215853 GSM3215853: scATAC-D6-50; Homo sapiens; ATAC-seq SRP151379 SRS3467549 GSM3215853 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215853 GSM3215853 GEO Accession GSM3215853 SRX4302207 GSM3215854 GSM3215854: scATAC-D6-51; Homo sapiens; ATAC-seq SRP151379 SRS3467541 GSM3215854 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215854 GSM3215854 GEO Accession GSM3215854 SRX4302208 GSM3215855 GSM3215855: scATAC-D6-52; Homo sapiens; ATAC-seq SRP151379 SRS3467546 GSM3215855 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215855 GSM3215855 GEO Accession GSM3215855 SRX4302209 GSM3215856 GSM3215856: scATAC-D6-53; Homo sapiens; ATAC-seq SRP151379 SRS3467550 GSM3215856 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215856 GSM3215856 GEO Accession GSM3215856 SRX4302210 GSM3215857 GSM3215857: scATAC-D6-54; Homo sapiens; ATAC-seq SRP151379 SRS3467548 GSM3215857 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215857 GSM3215857 GEO Accession GSM3215857 SRX4302211 GSM3215858 GSM3215858: scATAC-D6-55; Homo sapiens; ATAC-seq SRP151379 SRS3467547 GSM3215858 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215858 GSM3215858 GEO Accession GSM3215858 SRX4302212 GSM3215859 GSM3215859: scATAC-D6-56; Homo sapiens; ATAC-seq SRP151379 SRS3467555 GSM3215859 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215859 GSM3215859 GEO Accession GSM3215859 SRX4302213 GSM3215860 GSM3215860: scATAC-D6-57; Homo sapiens; ATAC-seq SRP151379 SRS3467556 GSM3215860 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215860 GSM3215860 GEO Accession GSM3215860 SRX4302214 GSM3215861 GSM3215861: scATAC-D6-58; Homo sapiens; ATAC-seq SRP151379 SRS3467554 GSM3215861 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215861 GSM3215861 GEO Accession GSM3215861 SRX4302215 GSM3215862 GSM3215862: scATAC-D6-59; Homo sapiens; ATAC-seq SRP151379 SRS3467551 GSM3215862 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215862 GSM3215862 GEO Accession GSM3215862 SRX4302216 GSM3215863 GSM3215863: scATAC-D6-5; Homo sapiens; ATAC-seq SRP151379 SRS3467558 GSM3215863 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215863 GSM3215863 GEO Accession GSM3215863 SRX4302217 GSM3215864 GSM3215864: scATAC-D6-60; Homo sapiens; ATAC-seq SRP151379 SRS3467553 GSM3215864 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215864 GSM3215864 GEO Accession GSM3215864 SRX4302218 GSM3215865 GSM3215865: scATAC-D6-61; Homo sapiens; ATAC-seq SRP151379 SRS3467560 GSM3215865 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215865 GSM3215865 GEO Accession GSM3215865 SRX4302219 GSM3215866 GSM3215866: scATAC-D6-62; Homo sapiens; ATAC-seq SRP151379 SRS3467552 GSM3215866 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215866 GSM3215866 GEO Accession GSM3215866 SRX4302220 GSM3215867 GSM3215867: scATAC-D6-63; Homo sapiens; ATAC-seq SRP151379 SRS3467561 GSM3215867 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215867 GSM3215867 GEO Accession GSM3215867 SRX4302221 GSM3215868 GSM3215868: scATAC-D6-64; Homo sapiens; ATAC-seq SRP151379 SRS3467557 GSM3215868 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215868 GSM3215868 GEO Accession GSM3215868 SRX4302222 GSM3215869 GSM3215869: scATAC-D6-65; Homo sapiens; ATAC-seq SRP151379 SRS3467559 GSM3215869 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215869 GSM3215869 GEO Accession GSM3215869 SRX4302223 GSM3215870 GSM3215870: scATAC-D6-66; Homo sapiens; ATAC-seq SRP151379 SRS3467564 GSM3215870 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215870 GSM3215870 GEO Accession GSM3215870 SRX4302224 GSM3215871 GSM3215871: scATAC-D6-67; Homo sapiens; ATAC-seq SRP151379 SRS3467565 GSM3215871 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215871 GSM3215871 GEO Accession GSM3215871 SRX4302225 GSM3215872 GSM3215872: scATAC-D6-68; Homo sapiens; ATAC-seq SRP151379 SRS3467562 GSM3215872 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215872 GSM3215872 GEO Accession GSM3215872 SRX4302226 GSM3215873 GSM3215873: scATAC-D6-69; Homo sapiens; ATAC-seq SRP151379 SRS3467568 GSM3215873 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215873 GSM3215873 GEO Accession GSM3215873 SRX4302227 GSM3215874 GSM3215874: scATAC-D6-6; Homo sapiens; ATAC-seq SRP151379 SRS3467563 GSM3215874 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215874 GSM3215874 GEO Accession GSM3215874 SRX4302228 GSM3215875 GSM3215875: scATAC-D6-70; Homo sapiens; ATAC-seq SRP151379 SRS3467567 GSM3215875 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215875 GSM3215875 GEO Accession GSM3215875 SRX4302229 GSM3215876 GSM3215876: scATAC-D6-71; Homo sapiens; ATAC-seq SRP151379 SRS3467570 GSM3215876 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215876 GSM3215876 GEO Accession GSM3215876 SRX4302230 GSM3215877 GSM3215877: scATAC-D6-72; Homo sapiens; ATAC-seq SRP151379 SRS3467566 GSM3215877 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215877 GSM3215877 GEO Accession GSM3215877 SRX4302231 GSM3215878 GSM3215878: scATAC-D6-73; Homo sapiens; ATAC-seq SRP151379 SRS3467590 GSM3215878 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215878 GSM3215878 GEO Accession GSM3215878 SRX4302232 GSM3215879 GSM3215879: scATAC-D6-74; Homo sapiens; ATAC-seq SRP151379 SRS3467569 GSM3215879 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215879 GSM3215879 GEO Accession GSM3215879 SRX4302233 GSM3215880 GSM3215880: scATAC-D6-75; Homo sapiens; ATAC-seq SRP151379 SRS3467574 GSM3215880 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215880 GSM3215880 GEO Accession GSM3215880 SRX4302234 GSM3215881 GSM3215881: scATAC-D6-76; Homo sapiens; ATAC-seq SRP151379 SRS3467571 GSM3215881 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215881 GSM3215881 GEO Accession GSM3215881 SRX4302235 GSM3215882 GSM3215882: scATAC-D6-77; Homo sapiens; ATAC-seq SRP151379 SRS3467572 GSM3215882 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215882 GSM3215882 GEO Accession GSM3215882 SRX4302236 GSM3215883 GSM3215883: scATAC-D6-78; Homo sapiens; ATAC-seq SRP151379 SRS3467578 GSM3215883 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215883 GSM3215883 GEO Accession GSM3215883 SRX4302237 GSM3215884 GSM3215884: scATAC-D6-79; Homo sapiens; ATAC-seq SRP151379 SRS3467573 GSM3215884 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215884 GSM3215884 GEO Accession GSM3215884 SRX4302238 GSM3215885 GSM3215885: scATAC-D6-7; Homo sapiens; ATAC-seq SRP151379 SRS3467576 GSM3215885 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215885 GSM3215885 GEO Accession GSM3215885 SRX4302239 GSM3215886 GSM3215886: scATAC-D6-80; Homo sapiens; ATAC-seq SRP151379 SRS3467575 GSM3215886 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215886 GSM3215886 GEO Accession GSM3215886 SRX4302240 GSM3215887 GSM3215887: scATAC-D6-81; Homo sapiens; ATAC-seq SRP151379 SRS3467582 GSM3215887 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215887 GSM3215887 GEO Accession GSM3215887 SRX4302241 GSM3215888 GSM3215888: scATAC-D6-82; Homo sapiens; ATAC-seq SRP151379 SRS3467583 GSM3215888 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215888 GSM3215888 GEO Accession GSM3215888 SRX4302242 GSM3215889 GSM3215889: scATAC-D6-83; Homo sapiens; ATAC-seq SRP151379 SRS3467581 GSM3215889 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215889 GSM3215889 GEO Accession GSM3215889 SRX4302243 GSM3215890 GSM3215890: scATAC-D6-84; Homo sapiens; ATAC-seq SRP151379 SRS3467585 GSM3215890 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215890 GSM3215890 GEO Accession GSM3215890 SRX4302244 GSM3215891 GSM3215891: scATAC-D6-85; Homo sapiens; ATAC-seq SRP151379 SRS3467591 GSM3215891 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215891 GSM3215891 GEO Accession GSM3215891 SRX4302245 GSM3215892 GSM3215892: scATAC-D6-86; Homo sapiens; ATAC-seq SRP151379 SRS3467584 GSM3215892 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215892 GSM3215892 GEO Accession GSM3215892 SRX4302246 GSM3215893 GSM3215893: scATAC-D6-87; Homo sapiens; ATAC-seq SRP151379 SRS3467588 GSM3215893 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215893 GSM3215893 GEO Accession GSM3215893 SRX4302247 GSM3215894 GSM3215894: scATAC-D6-88; Homo sapiens; ATAC-seq SRP151379 SRS3467592 GSM3215894 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215894 GSM3215894 GEO Accession GSM3215894 SRX4302248 GSM3215895 GSM3215895: scATAC-D6-89; Homo sapiens; ATAC-seq SRP151379 SRS3467586 GSM3215895 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215895 GSM3215895 GEO Accession GSM3215895 SRX4302249 GSM3215896 GSM3215896: scATAC-D6-8; Homo sapiens; ATAC-seq SRP151379 SRS3467580 GSM3215896 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215896 GSM3215896 GEO Accession GSM3215896 SRX4302250 GSM3215897 GSM3215897: scATAC-D6-90; Homo sapiens; ATAC-seq SRP151379 SRS3467577 GSM3215897 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215897 GSM3215897 GEO Accession GSM3215897 SRX4302251 GSM3215898 GSM3215898: scATAC-D6-91; Homo sapiens; ATAC-seq SRP151379 SRS3467579 GSM3215898 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215898 GSM3215898 GEO Accession GSM3215898 SRX4302252 GSM3215899 GSM3215899: scATAC-D6-92; Homo sapiens; ATAC-seq SRP151379 SRS3466282 GSM3215899 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215899 GSM3215899 GEO Accession GSM3215899 SRX4302253 GSM3215900 GSM3215900: scATAC-D6-93; Homo sapiens; ATAC-seq SRP151379 SRS3466283 GSM3215900 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215900 GSM3215900 GEO Accession GSM3215900 SRX4302254 GSM3215901 GSM3215901: scATAC-D6-94; Homo sapiens; ATAC-seq SRP151379 SRS3467589 GSM3215901 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215901 GSM3215901 GEO Accession GSM3215901 SRX4302255 GSM3215902 GSM3215902: scATAC-D6-95; Homo sapiens; ATAC-seq SRP151379 SRS3467587 GSM3215902 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215902 GSM3215902 GEO Accession GSM3215902 SRX4302256 GSM3215903 GSM3215903: scATAC-D6-96; Homo sapiens; ATAC-seq SRP151379 SRS3466284 GSM3215903 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215903 GSM3215903 GEO Accession GSM3215903 SRX4302257 GSM3215904 GSM3215904: scATAC-D6-9; Homo sapiens; ATAC-seq SRP151379 SRS3466285 GSM3215904 ATAC-seq GENOMIC other Single cells were captured using the C1 Single-Cell Auto Prep IFC microfluidic chips and assayed using the single-cell ATAC-seq protocol. In a 96-well plate, 15 µL of harvested libraries were amplified in 50 µL PCR for an additional 14 cycles (1.25 µM custom Nextera dual-index PCR primers in 1x NEBnext High-Fidelity PCR Master Mix) using the following PCR conditions: 72°C for 5min; 98°C for 30 s; and thermocycling at 98°C for 10 s, 72°C for 30 s, and 72°C for 1 min. Pooled libraries were purified and quantified using qPCR prior to sequencing. NextSeq 500 gds 303215904 GSM3215904 GEO Accession GSM3215904