| ID: 127457015 | NANOG-H3K27ac hESC enhancer GRCh37_chr7:95943579-95944241 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96314267..96314929) | | |
| ID: 127457014 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:95773203-95774037 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96143891..96144725) | | |
| ID: 127457013 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:95772367-95773202 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96143055..96143890) | | |
| ID: 123956181 | Sharpr-MPRA regulatory region 3069 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96327517..96327811) | | |
| ID: 110121296 | eDlx#23 enhancer in SHFM1 region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96136568..96137161) | | |
| ID: 110121293 | eExon 17 DLX5/6 limb enhancer [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96096967..96098368) | | |
| ID: 110121292 | eExon 15 DLX5/6 limb enhancer [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96075777..96076384) | | |
| ID: 110121172 | VISTA enhancer hs1642 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96245535..96248789) | | |
| ID: 106481349 | RNA, U6 small nuclear 532, pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96330638..96330744) | | |
| ID: 100271184 | ribosomal protein L21 pseudogene 74 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96283313..96283853) | RPL21_30_821 | |
| ID: 693176 | microRNA 591 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96219662..96219756, complement) | MIRN591, hsa-mir-591 | |
| ID: 360173 | CYCS pseudogene 18 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96127827..96128062, complement) | HCP18 | |
| ID: 10165 | solute carrier family 25 member 13 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96120220..96322098, complement) | ARALAR2, CITRIN, CTLN2, NICCD | 603859 |
| ID: 1780 | dynein cytoplasmic 1 intermediate chain 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95772554..96110322) | DNCI1, DNCIC1 | 603772 |