ID: 132090790 | Neanderthal introgressed variant-containing enhancer experimental_109279 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91282403..91282572) | | |
ID: 132089709 | Neanderthal introgressed variant-containing enhancer experimental_109225 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91258587..91258756) | | |
ID: 132089708 | Neanderthal introgressed variant-containing enhancer experimental_109154 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91191831..91192000) | | |
ID: 132089707 | Neanderthal introgressed variant-containing enhancer experimental_109153 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91188365..91188534) | | |
ID: 130002060 | ATAC-STARR-seq lymphoblastoid silent region 20026 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91423770..91424169) | | |
ID: 130002059 | ATAC-STARR-seq lymphoblastoid silent region 20025 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91361649..91362088) | | |
ID: 130002058 | ATAC-STARR-seq lymphoblastoid active region 28586 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91208417..91208476) | | |
ID: 130002057 | ATAC-STARR-seq lymphoblastoid active region 28584 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91163240..91163289) | | |
ID: 130002056 | ATAC-STARR-seq lymphoblastoid active region 28583 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91147736..91147855) | | |
ID: 129662472 | ReSE screen-validated silencer GRCh37_chr9:94188762-94188958 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91426480..91426676) | | |
ID: 129390093 | MPRA-validated peak7289 silencer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91364833..91365033) | | |
ID: 127815183 | NANOG hESC enhancer GRCh37_chr9:94106111-94106766 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91343829..91344484) | | |
ID: 127815182 | OCT4-H3K4me1 hESC enhancer GRCh37_chr9:94077443-94077942 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91315161..91315660) | | |
ID: 127815181 | OCT4-H3K4me1 hESC enhancer GRCh37_chr9:94076941-94077442 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91314659..91315160) | | |
ID: 127815180 | OCT4-NANOG hESC enhancer GRCh37_chr9:93979563-93980163 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91217281..91217881) | | |
ID: 127815179 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:93956125-93956992 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91193680..91194710) | | |
ID: 127815178 | NANOG-H3K4me1 hESC enhancer GRCh37_chr9:93909043-93909610 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91146761..91147328) | | |
ID: 127815177 | H3K4me1 hESC enhancer GRCh37_chr9:93833179-93834084 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91070897..91071802) | | |
ID: 124902209 | uncharacterized LOC124902209 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91421622..91422059) | | |
ID: 124902208 | uncharacterized LOC124902208 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (91193022..91198394) | | |