| ID: 132089669 | Neanderthal introgressed variant-containing enhancer experimental_107194 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18091370..18091539) | | |
| ID: 127814491 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:18438649-18439204 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18438651..18439206) | | |
| ID: 127814490 | NANOG hESC enhancer GRCh37_chr9:18366642-18367143 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18366644..18367145) | | |
| ID: 127814489 | OCT4-NANOG hESC enhancer GRCh37_chr9:18333062-18333625 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18333064..18333627) | | |
| ID: 127814488 | NANOG hESC enhancer GRCh37_chr9:18285808-18286309 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18285810..18286311) | | |
| ID: 127814487 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:17907351-17907895 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17907353..17907897) | | |
| ID: 127814486 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:17906806-17907350 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17906808..17907352) | | |
| ID: 126860587 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:18071016-18072215 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18071018..18072217) | | |
| ID: 114827838 | VISTA enhancer hs2537 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18361106..18364177) | | |
| ID: 107986990 | uncharacterized LOC107986990 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18344457..18384190) | | |
| ID: 105375987 | uncharacterized LOC105375987 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17902147..17907256, complement) | | |
| ID: 105369293 | uncharacterized LOC105369293 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18413781..18437504, complement) | | |
| ID: 100422869 | microRNA 3152 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18573306..18573379) | | |
| ID: 100421790 | pseudouridylate synthase 7 pseudogene 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (18153568..18154216) | | |
| ID: 92949 | ADAMTS like 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17906633..18910950) | ADAMTSL-1, ADAMTSR1, C9orf94, PUNCTIN | 609198 |