| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:67343855-67343930 | Rare:28 | ||||
| chr8:69492917-69493106 | Rare:47 | ||||
| chr8:70403791-70403904 | Rare:48 | ||||
| chr8:70607636-70607884 | Common:4; Rare:73 | ||||
| chr8:70608154-70608479 | Common:3; Rare:99 | ||||
| chr8:70669116-70669350 | Common:2; Rare:87 | ||||
| chr8:71844012-71844162 | Rare:62 | ||||
| chr8:73092954-73093256 | Common:4; Rare:100 | ||||
| chr8:73291622-73291863 | Rare:74 | ||||
| chr8:73292238-73292700 | Common:3; Rare:148 | ||||
| chr8:73294429-73294613 | Common:1; Rare:69 | ||||
| chr8:73878820-73879022 | Common:3; Rare:96 | ||||
| chr8:73972100-73972484 | Common:2; Rare:111 | ||||
| chr8:73976005-73976337 | Common:7; Rare:118; Clinvar:3; Clinvar (benign):4 | ||||
| chr8:74350317-74350464 | Common:1; Rare:59; Clinvar (benign):2 |