SRX1841246 GSM2199332 SRP076491 SRS1500427 GSM2199332 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199332 GEO Accession GSM2199332 SRX1841247 GSM2199333 SRP076491 SRS1500428 GSM2199333 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199333 GEO Accession GSM2199333 SRX1841248 GSM2199334 SRP076491 SRS1500429 GSM2199334 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199334 GEO Accession GSM2199334 SRX1841249 GSM2199335 SRP076491 SRS1500430 GSM2199335 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199335 GEO Accession GSM2199335 SRX1841250 GSM2199336 SRP076491 SRS1500431 GSM2199336 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. Purified cells were sorted a second time to further enrich for GFP-positive cells. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199336 GEO Accession GSM2199336 SRX1841251 GSM2199337 SRP076491 SRS1500432 GSM2199337 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. Purified cells were sorted a second time to further enrich for GFP-positive cells. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199337 GEO Accession GSM2199337 SRX1841252 GSM2199338 SRP076491 SRS1500433 GSM2199338 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199338 GEO Accession GSM2199338 SRX1841253 GSM2199339 SRP076491 SRS1500434 GSM2199339 OTHER GENOMIC other Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in 10% FBS in PBS. ATAC-seq libraries were prepared using the standard protocol (Buenrostro et al. 2013). Illumina HiSeq 2500 gds 302199339 GEO Accession GSM2199339 SRX1841254 GSM2199340 SRP076491 SRS1500435 GSM2199340 RNA-Seq TRANSCRIPTOMIC cDNA Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in Buffer RLT (Qiagen). cDNA was prepared using the SMARTer Ultra Low RNA Kit for Illumina Sequencing - HV (Clontech) per manufacturer's instructions. Subsequent preparation of RNA-seq libraries was performed using standard Illumina protocols. Illumina HiSeq 2500 gds 302199340 GEO Accession GSM2199340 SRX1841255 GSM2199341 SRP076491 SRS1500436 GSM2199341 RNA-Seq TRANSCRIPTOMIC cDNA Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in Buffer RLT (Qiagen). cDNA was prepared using the SMARTer Ultra Low RNA Kit for Illumina Sequencing - HV (Clontech) per manufacturer's instructions. Subsequent preparation of RNA-seq libraries was performed using standard Illumina protocols. Illumina HiSeq 2500 gds 302199341 GEO Accession GSM2199341 SRX1841256 GSM2199342 SRP076491 SRS1500437 GSM2199342 RNA-Seq TRANSCRIPTOMIC cDNA Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in Buffer RLT (Qiagen). cDNA was prepared using the SMARTer Ultra Low RNA Kit for Illumina Sequencing - HV (Clontech) per manufacturer's instructions. Subsequent preparation of RNA-seq libraries was performed using standard Illumina protocols. Illumina HiSeq 2500 gds 302199342 GEO Accession GSM2199342 SRX1841257 GSM2199343 SRP076491 SRS1500438 GSM2199343 RNA-Seq TRANSCRIPTOMIC cDNA Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in Buffer RLT (Qiagen). cDNA was prepared using the SMARTer Ultra Low RNA Kit for Illumina Sequencing - HV (Clontech) per manufacturer's instructions. Subsequent preparation of RNA-seq libraries was performed using standard Illumina protocols. Illumina HiSeq 2500 gds 302199343 GEO Accession GSM2199343 SRX1841258 GSM2199344 SRP076491 SRS1500439 GSM2199344 RNA-Seq TRANSCRIPTOMIC cDNA Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in Buffer RLT (Qiagen). cDNA was prepared using the SMARTer Ultra Low RNA Kit for Illumina Sequencing - HV (Clontech) per manufacturer's instructions. Subsequent preparation of RNA-seq libraries was performed using standard Illumina protocols. Illumina HiSeq 2500 gds 302199344 GEO Accession GSM2199344 SRX1841259 GSM2199345 SRP076491 SRS1500440 GSM2199345 RNA-Seq TRANSCRIPTOMIC cDNA Retinas were harvested from eight-week-old mice, dissociated with trypsin, washed with calcium- and magnesium-free HBSS, and resuspended in FACS buffer (1% FBS, 0.1mM EDTA in calcium- and magnesium-free HBSS). GFP-positive cells were isolated via FACS and collected in Buffer RLT (Qiagen). cDNA was prepared using the SMARTer Ultra Low RNA Kit for Illumina Sequencing - HV (Clontech) per manufacturer's instructions. Subsequent preparation of RNA-seq libraries was performed using standard Illumina protocols. Illumina HiSeq 2500 gds 302199345 GEO Accession GSM2199345