| ID: 127814996 | OCT4-NANOG hESC enhancer GRCh37_chr9:81976953-81977508 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79362038..79362593) | | |
| ID: 127814995 | OCT4-NANOG hESC enhancer GRCh37_chr9:81975510-81976401 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79360595..79361486) | | |
| ID: 126860651 | MED14-independent group 3 enhancer GRCh37_chr9:81640860-81642059 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79025944..79027143) | | |
| ID: 126860650 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:81637359-81638558 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79022443..79023642) | | |
| ID: 126860649 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:81486161-81487360 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (78871245..78872444) | | |
| ID: 124906889 | uncharacterized LOC124906889 [Homo sapiens (human)] | | | |
| ID: 124906888 | uncharacterized LOC124906888 [Homo sapiens (human)] | | | |
| ID: 124902186 | uncharacterized LOC124902186 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79201207..79208829) | | |
| ID: 113839563 | Sharpr-MPRA regulatory region 1407 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (78970453..78970747) | | |
| ID: 110120764 | VISTA enhancer hs765 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79208382..79209752) | | |
| ID: 110120661 | VISTA enhancer hs313 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79255707..79257309) | | |
| ID: 105376097 | uncharacterized LOC105376097 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (78861022..78882043, complement) | | |
| ID: 101927450 | uncharacterized LOC101927450 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79135422..79145666, complement) | | |
| ID: 645345 | coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 9 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79391267..79392035) | C9orf49, CHCHD9 | |
| ID: 340460 | keratin 18 pseudogene 24 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (79036353..79037748, complement) | | |