| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47960112-47960280 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr8:47960804-47960990 | Common:1; Rare:71; Clinvar:6 | ||||
| chr8:48008220-48008457 | Common:2; Rare:112 | ||||
| chr8:51898955-51899331 | Common:7; Rare:165 | ||||
| chr8:51899603-51899649 | Rare:7 | ||||
| chr8:52714377-52714616 | Common:1; Rare:106 | ||||
| chr8:53843207-53843350 | Rare:35 | ||||
| chr8:54021921-54022061 | Rare:66 | ||||
| chr8:54022246-54022563 | Common:1; Rare:103 | ||||
| chr8:54101776-54102129 | Common:3; Rare:147 | ||||
| chr8:54135117-54135308 | Common:3; Rare:63 | ||||
| chr8:54457721-54457946 | Common:1; Rare:54 | ||||
| chr8:55773306-55773678 | Common:4; Rare:132 | ||||
| chr8:56074371-56074867 | Common:11; Rare:166 | ||||
| chr8:58552871-58553297 | Common:1; Rare:109 |