| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:97868837-97869152 | Common:1; Rare:65 | ||||
| chr8:98016388-98016657 | Common:2; Rare:65 | ||||
| chr8:98032137-98032317 | Common:2; Rare:32 | ||||
| chr8:98045345-98045660 | Common:3; Rare:96 | ||||
| chr8:98117098-98117325 | Common:2; Rare:82 | ||||
| chr8:99012495-99012838 | Rare:65 | ||||
| chr8:99013007-99013400 | Rare:80; Clinvar:1 | ||||
| chr8:100150564-100150708 | Rare:44 | ||||
| chr8:100309892-100310315 | Common:1; Rare:159 | ||||
| chr8:100951265-100951438 | Rare:63 | ||||
| chr8:101492291-101492474 | Common:1; Rare:32 | ||||
| chr8:101492514-101492784 | Common:1; Rare:59; Clinvar (benign):2 | ||||
| chr8:101790892-101791107 | Rare:35 | ||||
| chr8:102239026-102239328 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr8:103298702-103298933 | Common:1; Rare:57 |