| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47960668-47961004 | Common:2; Rare:130; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:48008321-48008455 | Common:2; Rare:85 | ||||
| chr8:48735225-48735420 | Common:3; Rare:46 | ||||
| chr8:51898940-51899347 | Common:8; Rare:182 | ||||
| chr8:52254338-52254442 | Rare:23 | ||||
| chr8:52714427-52714626 | Common:1; Rare:86 | ||||
| chr8:53842949-53843047 | Rare:29 | ||||
| chr8:53843207-53843355 | Rare:35 | ||||
| chr8:54022070-54022557 | Common:1; Rare:164 | ||||
| chr8:54101769-54102139 | Common:3; Rare:153 | ||||
| chr8:54135117-54135314 | Common:3; Rare:65 | ||||
| chr8:55772990-55773093 | Rare:28 | ||||
| chr8:55773261-55773695 | Common:4; Rare:148 | ||||
| chr8:56074374-56074741 | Common:7; Rare:146 | ||||
| chr8:58411258-58411466 | Common:3; Rare:69 |