ID: 130001943 | ATAC-STARR-seq lymphoblastoid silent region 19983 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84261213..84261272) | | |
ID: 130001942 | ATAC-STARR-seq lymphoblastoid silent region 19981 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980189..83980328) | | |
ID: 130001941 | ATAC-STARR-seq lymphoblastoid active region 28497 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83979489..83979648) | | |
ID: 127815049 | NANOG hESC enhancer GRCh37_chr9:86891619-86892170 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84276704..84277255) | | |
ID: 127815048 | H3K4me1 hESC enhancer GRCh37_chr9:86787894-86788403 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84172979..84173488) | | |
ID: 127815047 | OCT4-NANOG hESC enhancer GRCh37_chr9:86766071-86767007 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84151156..84152092) | | |
ID: 127815046 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86595901-86596409 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980986..83981494) | | |
ID: 127815045 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86595393-86595900 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980469..83980985) | | |
ID: 126860658 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:86892303-86893502 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84277388..84278587) | | |
ID: 124310575 | Sharpr-MPRA regulatory region 11289 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84206214..84206508) | | |
ID: 123706516 | HNRNPK antisense RNA 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83972095..83975780) | | |
ID: 105376116 | SLC28A3 regulatory antisense RNA 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84278170..84290136) | | |
ID: 101927575 | uncharacterized LOC101927575 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84063443..84094601) | | |
ID: 100874474 | high mobility group nucleosomal binding domain 2 pseudogene 33 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84078517..84079057) | | |
ID: 407043 | microRNA 7-1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83969748..83969857, complement) | MIRN7-1, hsa-mir-7-1, mir-7-1 | 615239 |
ID: 80010 | RecQ mediated genome instability 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980359..84004074) | BLAP75, C9orf76, FAAP75 | 610404 |
ID: 64078 | solute carrier family 28 member 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84275457..84368727, complement) | CNT3 | 608269 |
ID: 3190 | heterogeneous nuclear ribonucleoprotein K [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83968083..83980615, complement) | AUKS, CSBP, HNRPK, TUNP | 600712 |