| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121696919-121697198 | Common:4; Rare:81 | ||||
| chr4:121801240-121801411 | Common:2; Rare:57 | ||||
| chr4:121823835-121824076 | Common:2; Rare:59 | ||||
| chr4:121870413-121870651 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr4:122732436-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922897-122923139 | Common:2; Rare:68 | ||||
| chr4:123399593-123399656 | Rare:19 | ||||
| chr4:127632760-127632966 | Common:1; Rare:49 | ||||
| chr4:127880764-127880939 | Rare:62 | ||||
| chr4:129093441-129093736 | Common:2; Rare:83 | ||||
| chr4:137532402-137532829 | Common:2; Rare:77 | ||||
| chr4:139301269-139301543 | Common:4; Rare:81 | ||||
| chr4:139453665-139454185 | Common:5; Rare:144; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556188-139556357 | Rare:38 | ||||
| chr4:140373393-140373701 | Common:2; Rare:127 |