| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139665912-139666026 | Common:1; Rare:34 | ||||
| chr4:140373357-140373713 | Common:3; Rare:141 | ||||
| chr4:141220856-141220993 | Rare:52 | ||||
| chr4:141636568-141636589 | Rare:3 | ||||
| chr4:141636766-141636915 | Common:1; Rare:34 | ||||
| chr4:143184652-143184998 | Common:8; Rare:137 | ||||
| chr4:143513348-143513544 | Common:2; Rare:70 | ||||
| chr4:145098141-145098364 | Rare:78 | ||||
| chr4:145619320-145619396 | Rare:30 | ||||
| chr4:147480883-147481028 | Rare:29 | ||||
| chr4:147617256-147617455 | Common:1; Rare:44 | ||||
| chr4:147684127-147684296 | Rare:70 | ||||
| chr4:148442307-148442712 | Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581731-150581944 | Rare:42 | ||||
| chr4:151015718-151015861 | Rare:69 |