| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112637408-112637570 | Common:3; Rare:44 | ||||
| chr4:118685310-118685440 | Common:2; Rare:42 | ||||
| chr4:119212410-119212720 | Common:2; Rare:94 | ||||
| chr4:120066736-120066973 | Common:4; Rare:71 | ||||
| chr4:121801254-121801473 | Common:2; Rare:74; Clinvar (pathogenic):1 | ||||
| chr4:122732436-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922897-122923163 | Common:2; Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:127880811-127880939 | Rare:40 | ||||
| chr4:129093441-129093741 | Common:2; Rare:85 | ||||
| chr4:133149078-133149301 | Common:2; Rare:68 | ||||
| chr4:138242332-138242559 | Common:1; Rare:49 | ||||
| chr4:139301224-139301557 | Common:4; Rare:96 | ||||
| chr4:139453950-139454132 | Common:2; Rare:53; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:140373380-140373709 | Common:3; Rare:133 | ||||
| chr4:142405394-142405537 | Rare:23 |