| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:101492602-101492784 | Common:1; Rare:36; Clinvar (benign):2 | ||||
| chr8:102238781-102238869 | Common:1; Rare:40; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:102239058-102239331 | Common:2; Rare:58 | ||||
| chr8:102412242-102412580 | Common:1; Rare:99 | ||||
| chr8:102412692-102412948 | Common:3; Rare:62 | ||||
| chr8:102864146-102864293 | Rare:65 | ||||
| chr8:103298724-103298904 | Common:1; Rare:43 | ||||
| chr8:103415046-103415516 | Common:6; Rare:236 | ||||
| chr8:106657559-106657979 | Common:5; Rare:120 | ||||
| chr8:108443471-108443653 | Common:2; Rare:79 | ||||
| chr8:109334060-109334406 | Common:1; Rare:86 | ||||
| chr8:115668946-115669236 | Rare:67 | ||||
| chr8:116766350-116766577 | Common:2; Rare:54 | ||||
| chr8:116874388-116874668 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr8:116938394-116938535 | Common:6; Rare:57 |