| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066754-120066904 | Common:1; Rare:48 | ||||
| chr4:120066911-120067010 | Common:3; Rare:25 | ||||
| chr4:121072246-121072456 | Rare:57 | ||||
| chr4:121381010-121381186 | Rare:45 | ||||
| chr4:121696916-121697133 | Common:4; Rare:59 | ||||
| chr4:121765115-121765213 | Common:1; Rare:32 | ||||
| chr4:121765333-121765389 | Rare:11 | ||||
| chr4:121765435-121765561 | Rare:24 | ||||
| chr4:121801252-121801439 | Common:2; Rare:59 | ||||
| chr4:121823835-121824121 | Common:2; Rare:72 | ||||
| chr4:122152225-122152429 | Common:2; Rare:88 | ||||
| chr4:122732408-122732768 | Common:2; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922896-122923148 | Common:2; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396668-123396863 | Rare:51 | ||||
| chr4:123399338-123399662 | Common:1; Rare:98 |