| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:99661187-99661437 | Common:1; Rare:56; Clinvar (pathogenic):2 | ||||
| chr8:99835492-99835560 | Rare:27; Clinvar (pathogenic):1 | ||||
| chr8:100292822-100292980 | Rare:32 | ||||
| chr8:100464047-100464324 | Common:1; Rare:47 | ||||
| chr8:101493802-101494004 | Common:2; Rare:55 | ||||
| chr8:102656434-102656508 | Common:1; Rare:20 | ||||
| chr8:103318312-103318729 | Rare:86; Clinvar:1 | ||||
| chr8:103499183-103499290 | Common:1; Rare:16 | ||||
| chr8:109333467-109333594 | Rare:22 | ||||
| chr8:117764269-117764555 | Common:5; Rare:62 | ||||
| chr8:117897647-117897658 | Rare:4 | ||||
| chr8:117946583-117946819 | Common:2; Rare:41 | ||||
| chr8:118011810-118011930 | Rare:17 | ||||
| chr8:118296441-118296554 | Common:1; Rare:16 | ||||
| chr8:118327383-118327599 | Rare:39 |