| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:101347528-101347826 | Common:5; Rare:92 | ||||
| chr4:102760898-102761053 | Rare:52; Clinvar:1 | ||||
| chr4:102826768-102827187 | Common:4; Rare:139 | ||||
| chr4:102827445-102828142 | Common:4; Rare:233 | ||||
| chr4:102868834-102869059 | Common:2; Rare:76 | ||||
| chr4:103076303-103076372 | Rare:22 | ||||
| chr4:105146545-105146912 | Common:2; Rare:118 | ||||
| chr4:105708641-105708827 | Rare:59 | ||||
| chr4:106316169-106316612 | Common:5; Rare:142 | ||||
| chr4:107720175-107720544 | Common:7; Rare:151 | ||||
| chr4:107824468-107824740 | Common:1; Rare:54 | ||||
| chr4:107824793-107825035 | Common:1; Rare:68 | ||||
| chr4:107989679-107989942 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620384-108620621 | Common:6; Rare:119 | ||||
| chr4:109433757-109433924 | Common:1; Rare:58 |