SRX18392426 LEN1 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876540 LEN1 LEN1 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392427 LSN1 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876542 LSN1 LSN1 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392428 MT4 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876541 MT4 MT4 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392429 CC76 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876543 CC76 CC76 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392430 CC89 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876544 CC89 CC89 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392431 BLC1 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876545 BLC1 BLC1 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392432 CC86 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876546 CC86 CC86 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392433 CC102 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876547 CC102 CC102 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392434 MN-9 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876548 MN-9 MN-9 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392435 MN-1 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876549 MN-1 MN-1 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392436 MN-2 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876550 MN-2 MN-2 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392437 MN-6 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876551 MN-6 MN-6 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392438 CC_87 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876552 CC_87 CC_87 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392439 CC101 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876553 CC101 CC101 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392440 LET1 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876554 LET1 LET1 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550 SRX18392441 LST1 SRP410072 bp0 RNA sequencing was performed according to the previous protocol used to generate ANTE collection of healthy tissue RNAseq profiles (Suntsova et al (2019)). To isolate RNA preps, 10 M-thick paraffin slices were trimmed from each FFPE tissue block with a microtome. RNA was extracted from FFPE slices using QIAGEN RNeasy FFPE Kit following the manufacturers protocol. RNA 6000 Nano or Qubit RNA Assay kits were used to measure RNA concentration. RNA Integrity Number (RIN) was measured using Agilent 2100 bio-Analyzer. For depletion of ribosomal RNA and library construction, KAPA RNA Hyper with rRNA erase kit (HMR only) was used. Different adaptors were used for multiplexing samples in a single sequencing run. Library concentrations were measured using the Qubit ds DNA HS Assay kit (Life Technologies) and Agilent Tapestation (Agilent). RNA sequencing was performed using Illumina NextSeq550 equipment for single-end sequencing, 70 bp read length). SRS15876555 LST1 LST1 RNA-Seq TRANSCRIPTOMIC cDNA NextSeq 550