ID: 132089723 | Neanderthal introgressed variant-containing enhancer experimental_110085 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94154169..94154338) | | |
ID: 132089722 | Neanderthal introgressed variant-containing enhancer experimental_110072 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94153863..94154032) | | |
ID: 132089721 | Neanderthal introgressed variant-containing enhancer experimental_110048 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94141102..94141271) | | |
ID: 132089720 | Neanderthal introgressed variant-containing enhancer experimental_110021 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93966469..93966638) | | |
ID: 130002113 | ATAC-STARR-seq lymphoblastoid silent region 20054 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94171166..94171215) | | |
ID: 130002112 | ATAC-STARR-seq lymphoblastoid silent region 20053 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94166913..94166982) | | |
ID: 130002111 | ATAC-STARR-seq lymphoblastoid silent region 20051 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94030672..94031091) | | |
ID: 130002110 | ATAC-STARR-seq lymphoblastoid active region 28627 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94030352..94030401) | | |
ID: 127815309 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:96880956-96881652 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94118674..94119370) | | |
ID: 127815308 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:96856496-96857248 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94094214..94094966) | | |
ID: 127815307 | H3K4me1 hESC enhancer GRCh37_chr9:96741809-96742308 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93979527..93980026) | | |
ID: 127815306 | H3K4me1 hESC enhancer GRCh37_chr9:96730989-96731521 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93968707..93969239) | | |
ID: 127815305 | H3K4me1 hESC enhancer GRCh37_chr9:96718163-96718693 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93955881..93956411) | | |
ID: 127815304 | H3K4me1 hESC enhancer GRCh37_chr9:96717631-96718162 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93955349..93955880) | | |
ID: 127815303 | H3K4me1 hESC enhancer GRCh37_chr9:96715656-96716219 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93953374..93953937) | | |
ID: 127815302 | H3K4me1 hESC enhancer GRCh37_chr9:96715091-96715655 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93952809..93953373) | | |
ID: 126860684 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:96767229-96768428 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94004947..94006146) | | |
ID: 126860683 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:96748340-96749539 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93986058..93987257) | | |
ID: 124902216 | uncharacterized LOC124902216 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93955526..93980654) | | |
ID: 124310590 | Sharpr-MPRA regulatory region 768 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94084387..94084681) | | |