SRX2162574 GSM2310074 SRP089822 PRJNA342855 SRS1690625 SAMN05770371 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310074 GSM2310074 GEO Accession GSM2310074 SRX2162575 GSM2310075 SRP089822 PRJNA342855 SRS1690626 SAMN05770370 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310075 GSM2310075 GEO Accession GSM2310075 SRX2162576 GSM2310076 SRP089822 PRJNA342855 SRS1690627 SAMN05770369 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310076 GSM2310076 GEO Accession GSM2310076 SRX2162577 GSM2310077 SRP089822 PRJNA342855 SRS1690628 SAMN05770368 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310077 GSM2310077 GEO Accession GSM2310077 SRX2162578 GSM2310078 SRP089822 PRJNA342855 SRS1690629 SAMN05770367 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310078 GSM2310078 GEO Accession GSM2310078 SRX2162579 GSM2310079 SRP089822 PRJNA342855 SRS1690630 SAMN05770388 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310079 GSM2310079 GEO Accession GSM2310079 SRX2162580 GSM2310080 SRP089822 PRJNA342855 SRS1690631 SAMN05770387 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310080 GSM2310080 GEO Accession GSM2310080 SRX2162581 GSM2310081 SRP089822 PRJNA342855 SRS1690632 SAMN05770386 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310081 GSM2310081 GEO Accession GSM2310081 SRX2162582 GSM2310082 SRP089822 PRJNA342855 SRS1690633 SAMN05770385 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310082 GSM2310082 GEO Accession GSM2310082 SRX2162583 GSM2310083 SRP089822 PRJNA342855 SRS1690634 SAMN05770384 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310083 GSM2310083 GEO Accession GSM2310083 SRX2162584 GSM2310084 SRP089822 PRJNA342855 SRS1690635 SAMN05770383 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310084 GSM2310084 GEO Accession GSM2310084 SRX2162585 GSM2310085 SRP089822 PRJNA342855 SRS1690636 SAMN05770382 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310085 GSM2310085 GEO Accession GSM2310085 SRX2162586 GSM2310086 SRP089822 PRJNA342855 SRS1690637 SAMN05770381 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310086 GSM2310086 GEO Accession GSM2310086 SRX2162587 GSM2310087 SRP089822 PRJNA342855 SRS1690638 SAMN05770380 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310087 GSM2310087 GEO Accession GSM2310087 SRX2162588 GSM2310088 SRP089822 PRJNA342855 SRS1690639 SAMN05770379 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310088 GSM2310088 GEO Accession GSM2310088 SRX2162589 GSM2310089 SRP089822 PRJNA342855 SRS1690640 SAMN05770378 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310089 GSM2310089 GEO Accession GSM2310089 SRX2162590 GSM2310090 SRP089822 PRJNA342855 SRS1690641 SAMN05770377 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310090 GSM2310090 GEO Accession GSM2310090 SRX2162591 GSM2310091 SRP089822 PRJNA342855 SRS1690642 SAMN05770376 OTHER GENOMIC other The genomic DNA of sorted cells were routinely extracted. The sequences corresponding to each shRNA were PCR amplified using universal primers, digested with XhoI and EcoRI restriction enzymes, and gel purified. The purified fragments were then used for preparation of a sequencing library according to the Illumina Hi-seq kit instructions. Illumina HiSeq 2000 gds 302310091 GSM2310091 GEO Accession GSM2310091