| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:101348060-101348136 | Rare:19 | ||||
| chr4:102760924-102761056 | Rare:45; Clinvar:1 | ||||
| chr4:102825528-102825555 | Rare:4 | ||||
| chr4:102868844-102869068 | Common:2; Rare:80 | ||||
| chr4:103076303-103076377 | Rare:24 | ||||
| chr4:103077241-103077399 | Rare:34 | ||||
| chr4:103198320-103198536 | Common:2; Rare:57 | ||||
| chr4:105708641-105708845 | Common:1; Rare:66 | ||||
| chr4:106316169-106316612 | Common:5; Rare:142 | ||||
| chr4:107720183-107720493 | Common:7; Rare:124 | ||||
| chr4:107824751-107825029 | Common:1; Rare:70 | ||||
| chr4:107989675-107989916 | Common:6; Rare:114; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620666 | Common:6; Rare:134 | ||||
| chr4:109433756-109433913 | Common:1; Rare:56 | ||||
| chr4:109730063-109730218 | Common:2; Rare:33 |