| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139302436-139302540 | Rare:26 | ||||
| chr4:139453653-139453749 | Common:2; Rare:35 | ||||
| chr4:139453770-139454204 | Common:3; Rare:112; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556148-139556522 | Rare:72 | ||||
| chr4:139606669-139607004 | Rare:74 | ||||
| chr4:139665564-139666026 | Common:2; Rare:94 | ||||
| chr4:140154062-140154288 | Common:1; Rare:85 | ||||
| chr4:140373357-140373732 | Common:3; Rare:148 | ||||
| chr4:140427598-140427694 | Common:1; Rare:19 | ||||
| chr4:141636560-141637156 | Common:1; Rare:134 | ||||
| chr4:142405394-142405493 | Rare:19 | ||||
| chr4:143184624-143184988 | Common:9; Rare:144 | ||||
| chr4:143513349-143513859 | Common:3; Rare:168 | ||||
| chr4:143513870-143514026 | Rare:72 | ||||
| chr4:145098117-145098379 | Rare:83 |