| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119628043-119628102 | Rare:16 | ||||
| chr4:120066784-120066964 | Common:4; Rare:51 | ||||
| chr4:120922683-120922944 | Rare:74; Clinvar:4 | ||||
| chr4:121696850-121697198 | Common:5; Rare:98 | ||||
| chr4:121801252-121801411 | Common:2; Rare:50 | ||||
| chr4:121823858-121824121 | Common:2; Rare:68 | ||||
| chr4:121870406-121870626 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr4:122152257-122152458 | Common:2; Rare:79 | ||||
| chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122826938-122827279 | Common:1; Rare:114; Clinvar (benign):1 | ||||
| chr4:122922545-122922699 | Common:2; Rare:72 | ||||
| chr4:122922945-122923184 | Common:2; Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396622-123396939 | Rare:74 | ||||
| chr4:123399322-123399561 | Common:1; Rare:75 | ||||
| chr4:123399593-123399779 | Common:1; Rare:42 |