| ID: 127823757 | H3K4me1 hESC enhancer GRCh37_chr12:16762919-16763418 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16609985..16610484) | | |
| ID: 127823756 | H3K4me1 hESC enhancer GRCh37_chr12:16757530-16758030 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16604596..16605096) | | |
| ID: 127823755 | NANOG hESC enhancer GRCh37_chr12:16703865-16704366 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16550931..16551432) | | |
| ID: 127823754 | OCT4-NANOG hESC enhancer GRCh37_chr12:16603467-16604039 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16450533..16451105) | | |
| ID: 127823753 | OCT4-NANOG hESC enhancer GRCh37_chr12:16602892-16603466 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16449958..16450532) | | |
| ID: 127823752 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:16535886-16536478 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16382952..16383544) | | |
| ID: 127823751 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:16535292-16535885 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16382358..16382951) | | |
| ID: 127823750 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:16501529-16502458 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16348595..16349524) | | |
| ID: 127823749 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:16499669-16500598 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16346735..16347664) | | |
| ID: 126861470 | MED14-independent group 3 enhancer GRCh37_chr12:17135721-17136920 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16982787..16983986) | | |
| ID: 124625916 | Sharpr-MPRA regulatory region 9686 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16359895..16360189) | | |
| ID: 124625915 | Sharpr-MPRA regulatory region 3277 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16030875..16031169) | | |
| ID: 110120934 | VISTA enhancer hs798 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16017656..16018890) | | |
| ID: 110120918 | VISTA enhancer hs661 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16787774..16789388) | | |
| ID: 110120907 | VISTA enhancer hs607 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16457111..16459002) | | |
| ID: 110120854 | VISTA enhancer hs336 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16562381..16563426) | | |
| ID: 105369677 | uncharacterized LOC105369677 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16787921..16988633, complement) | | |
| ID: 101928362 | uncharacterized LOC101928362 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16107509..16276525) | | |
| ID: 100420503 | egl-9 family hypoxia-inducible factor 3 pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15971818..15972802, complement) | | |
| ID: 729025 | solute carrier family 15 member 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16188485..16277685, complement) | | 620324 |