| ID: 132088793 | Neanderthal introgressed variant-containing enhancer experimental_55577 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163352449..163352618) | | |
| ID: 132088792 | Neanderthal introgressed variant-containing enhancer experimental_55575 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163349071..163349240) | | |
| ID: 129935041 | ATAC-STARR-seq lymphoblastoid active region 16725 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (164252782..164253011) | | |
| ID: 129935040 | ATAC-STARR-seq lymphoblastoid active region 16724 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (164015628..164015777) | | |
| ID: 129935039 | ATAC-STARR-seq lymphoblastoid active region 16723 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (164015538..164015587) | | |
| ID: 129660837 | ReSE screen-validated silencer GRCh37_chr2:165027147-165027366 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (164170637..164170856) | | |
| ID: 129660836 | ReSE screen-validated silencer GRCh37_chr2:164304809-164304985 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163448299..163448475) | | |
| ID: 127275136 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:164766241-164766758 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163909731..163910248) | | |
| ID: 127275135 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:164765722-164766240 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163909212..163909730) | | |
| ID: 127275134 | H3K27ac hESC enhancer GRCh37_chr2:164593642-164594157 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163737132..163737647) | | |
| ID: 127275133 | H3K27ac hESC enhancer GRCh37_chr2:164593125-164593641 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163736615..163737131) | | |
| ID: 127275132 | NANOG hESC enhancer GRCh37_chr2:164478034-164478535 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163621524..163622025) | | |
| ID: 127275131 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:164204489-164205088 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163347979..163348578) | | |
| ID: 126806395 | MED14-independent group 3 enhancer GRCh37_chr2:164809702-164810901 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163953192..163954391) | | |
| ID: 126806394 | MED14-independent group 3 enhancer GRCh37_chr2:164627636-164628835 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163771126..163772325) | | |
| ID: 122847308 | Sharpr-MPRA regulatory region 13497 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (164061159..164061453) | | |
| ID: 121725106 | Sharpr-MPRA regulatory region 10417 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163667679..163667973) | | |
| ID: 110120725 | VISTA enhancer hs640 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163717497..163718948) | | |
| ID: 110120677 | VISTA enhancer hs421 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163987287..163988273) | | |
| ID: 110120601 | VISTA enhancer hs170 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (163593634..163595248) | | |