| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:140755988-140756478 | Common:1; Rare:111 | ||||
| chr4:142474261-142474492 | Rare:40 | ||||
| chr4:142474498-142474565 | Rare:10 | ||||
| chr4:143184672-143184985 | Common:8; Rare:121 | ||||
| chr4:143336562-143336912 | Rare:79 | ||||
| chr4:143337236-143337384 | Rare:60 | ||||
| chr4:145098148-145098343 | Rare:69 | ||||
| chr4:145619327-145619406 | Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:146521859-146522028 | Rare:39 | ||||
| chr4:147617238-147617479 | Common:1; Rare:52 | ||||
| chr4:147684081-147684302 | Common:1; Rare:87 | ||||
| chr4:148442307-148442712 | Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151099544-151099713 | Common:3; Rare:77 | ||||
| chr4:151408874-151409257 | Common:5; Rare:122 | ||||
| chr4:151409349-151409452 | Common:1; Rare:19 |