ID: 130061451 | ATAC-STARR-seq lymphoblastoid active region 12601 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64848051..64848100) | | |
ID: 130061450 | ATAC-STARR-seq lymphoblastoid silent region 8852 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64836899..64837358) | | |
ID: 130061449 | ATAC-STARR-seq lymphoblastoid silent region 8851 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64836719..64836808) | | |
ID: 130061448 | ATAC-STARR-seq lymphoblastoid silent region 8850 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64781134..64781233) | | |
ID: 130061447 | ATAC-STARR-seq lymphoblastoid silent region 8849 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64780316..64780365) | | |
ID: 127887619 | H3K4me1 hESC enhancer GRCh37_chr17:62821718-62822218 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64825600..64826100) | | |
ID: 127887618 | H3K4me1 hESC enhancer GRCh37_chr17:62817908-62818408 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64821790..64822290) | | |
ID: 127887617 | H3K4me1 hESC enhancer GRCh37_chr17:62794173-62794673 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64798055..64798555) | | |
ID: 127887616 | H3K4me1 hESC enhancer GRCh37_chr17:62781097-62781856 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64784979..64785738) | | |
ID: 127887615 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:62774586-62775254 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64778468..64779136) | | |
ID: 127887614 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:62773916-62774585 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64777798..64778467) | | |
ID: 126862617 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:62782294-62783493 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64786110..64787375) | | |
ID: 109286553 | ARHGAP27P1-BPTFP1-KPNA2P3 readthrough, transcribed pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64749662..64781999, complement) | | |
ID: 109286551 | bromodomain PHD finger transcription factor pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64761914..64762712, complement) | | |
ID: 106479372 | RNA, 7SL, cytoplasmic 404, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64871504..64871784, complement) | | |
ID: 106479069 | RNA, U7 small nuclear 115 pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64825765..64825819, complement) | | |
ID: 105376844 | uncharacterized LOC105376844 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64849811..64909765) | | |
ID: 105371860 | uncharacterized LOC105371860 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64844396..64846757, complement) | | |
ID: 102929163 | ARF like GTPase 17A pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64870885..64882891) | | |
ID: 102464831 | microRNA 6080 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (64780759..64780824) | hsa-mir-6080 | |