| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121381010-121381137 | Rare:38 | ||||
| chr4:121696905-121697130 | Common:4; Rare:63 | ||||
| chr4:122152257-122152390 | Common:2; Rare:61 | ||||
| chr4:122732432-122732671 | Rare:67 | ||||
| chr4:122922933-122923128 | Common:2; Rare:56 | ||||
| chr4:128811174-128811317 | Rare:30 | ||||
| chr4:129093482-129093741 | Common:1; Rare:79 | ||||
| chr4:139301184-139301574 | Common:6; Rare:111 | ||||
| chr4:139453770-139454204 | Common:3; Rare:112; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373358-140373717 | Common:3; Rare:142 | ||||
| chr4:141220795-141221016 | Rare:74 | ||||
| chr4:141636757-141636898 | Common:1; Rare:37 | ||||
| chr4:143184646-143184998 | Common:9; Rare:139 | ||||
| chr4:145098148-145098348 | Rare:70 | ||||
| chr4:145619340-145619396 | Rare:19 |