| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:101348036-101348186 | Rare:44 | ||||
| chr4:102760924-102761040 | Rare:37; Clinvar:1 | ||||
| chr4:102825761-102825861 | Rare:26 | ||||
| chr4:102826720-102827002 | Rare:81 | ||||
| chr4:102827442-102828171 | Common:5; Rare:246 | ||||
| chr4:102868850-102869075 | Common:2; Rare:80 | ||||
| chr4:105708641-105708877 | Common:3; Rare:77 | ||||
| chr4:106316173-106316607 | Common:5; Rare:138 | ||||
| chr4:107720175-107720500 | Common:7; Rare:132 | ||||
| chr4:107824778-107825044 | Common:1; Rare:78 | ||||
| chr4:107989675-107989930 | Common:6; Rare:115; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620391-108620658 | Common:6; Rare:134 | ||||
| chr4:109433757-109433938 | Common:1; Rare:60 | ||||
| chr4:109560090-109560357 | Common:3; Rare:74 | ||||
| chr4:109730057-109730278 | Common:2; Rare:53 |