| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147617256-147617479 | Common:1; Rare:48 | ||||
| chr4:148442323-148442712 | Rare:110; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015220-151015292 | Rare:26 | ||||
| chr4:151409025-151409267 | Common:3; Rare:67 | ||||
| chr4:151760930-151761249 | Common:1; Rare:120 | ||||
| chr4:152779910-152780149 | Common:2; Rare:62 | ||||
| chr4:156971797-156971945 | Common:1; Rare:55 | ||||
| chr4:158172892-158173079 | Rare:29 | ||||
| chr4:158671830-158672139 | Common:4; Rare:82 | ||||
| chr4:158672208-158672489 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:168318774-168318856 | Rare:16 | ||||
| chr4:168480458-168480547 | Rare:18 | ||||
| chr4:169620360-169620954 | Common:2; Rare:169 | ||||
| chr4:173369787-173369935 | Common:1; Rare:50 | ||||
| chr4:173370617-173370988 | Common:2; Rare:92 |