ID: 132089651 | Neanderthal introgressed variant-containing enhancer experimental_105958 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111637638..111637807) | | |
ID: 132089650 | Neanderthal introgressed variant-containing enhancer experimental_105923 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111593909..111594078) | | |
ID: 132089649 | Neanderthal introgressed variant-containing enhancer experimental_105891 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111572853..111573022) | | |
ID: 132089648 | Neanderthal introgressed variant-containing enhancer experimental_105889 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111570763..111570932) | | |
ID: 130002367 | ATAC-STARR-seq lymphoblastoid active region 28798 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111662616..111662665) | | |
ID: 130002366 | ATAC-STARR-seq lymphoblastoid active region 28797 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111662316..111662415) | | |
ID: 130002365 | ATAC-STARR-seq lymphoblastoid silent region 20183 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111661906..111662025) | | |
ID: 130002364 | ATAC-STARR-seq lymphoblastoid silent region 20182 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111661426..111661875) | | |
ID: 130002363 | ATAC-STARR-seq lymphoblastoid active region 28796 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111661186..111661245) | | |
ID: 130002362 | ATAC-STARR-seq lymphoblastoid active region 28795 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111632018..111632067) | | |
ID: 130002361 | ATAC-STARR-seq lymphoblastoid silent region 20181 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111631378..111631667) | | |
ID: 130002360 | ATAC-STARR-seq lymphoblastoid active region 28794 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111631198..111631287) | | |
ID: 127815595 | NANOG-H3K27ac hESC enhancer GRCh37_chr9:114379051-114379784 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111616771..111617504) | | |
ID: 127815594 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:114361778-114362350 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111599498..111600070) | | |
ID: 121811716 | Sharpr-MPRA regulatory region 3205 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111678249..111678543) | | |
ID: 121331343 | Sharpr-MPRA regulatory region 12797 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111636789..111637083) | | |
ID: 111589207 | FOXA motif-containing MPRA enhancer 227 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111635047..111635191) | | |
ID: 107987116 | uncharacterized LOC107987116 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111626921..111631203, complement) | | |
ID: 652972 | leucine rich repeat containing 37 member A5, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111602831..111613553, complement) | C9orf29 | |
ID: 552891 | DNAJC25-GNG10 readthrough [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (111631334..111670226) | | |