| ID: 132089506 | Neanderthal introgressed variant-containing enhancer experimental_100136 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81683294..81683463) | | |
| ID: 129998726 | ATAC-STARR-seq lymphoblastoid active region 26212 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81924806..81924865) | | |
| ID: 129998725 | ATAC-STARR-seq lymphoblastoid active region 26211 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81845753..81845832) | | |
| ID: 129998724 | ATAC-STARR-seq lymphoblastoid silent region 18335 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81685175..81685224) | | |
| ID: 127456890 | OCT4-NANOG hESC enhancer GRCh37_chr7:81302077-81302610 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81672761..81673294) | | |
| ID: 127456889 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:81178878-81179442 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81549562..81550126) | | |
| ID: 126860087 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:81487648-81488847 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81858332..81859531) | | |
| ID: 126860086 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:81252185-81253384 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81622869..81624068) | | |
| ID: 124901687 | uncharacterized LOC124901687 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (82094755..82111294, complement) | | |
| ID: 106481709 | DEAD-box helicase 43 pseudogene 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81610884..81611407, complement) | | |
| ID: 105369146 | uncharacterized LOC105369146 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81515747..81561819, complement) | | |
| ID: 101927356 | CACNA2D1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (82009177..82029955) | | |
| ID: 100128317 | uncharacterized LOC100128317 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81576386..81691406, complement) | | |
| ID: 3082 | hepatocyte growth factor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81699010..81770047, complement) | DFNB39, F-TCFB, HPTA, SF, HGF | 142409 |
| ID: 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (81946444..82443956, complement) | CACNA2, CACNL2A, CCHL2A, DEE110, LINC01112, lncRNA-N3 | 114204 |