| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107720175-107720496 | Common:7; Rare:131 | ||||
| chr4:107824461-107824745 | Common:1; Rare:58 | ||||
| chr4:107824793-107825035 | Common:1; Rare:68 | ||||
| chr4:107989669-107989919 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620380-108620717 | Common:6; Rare:152 | ||||
| chr4:109433756-109433947 | Common:1; Rare:63 | ||||
| chr4:109560076-109560389 | Common:5; Rare:89 | ||||
| chr4:109703408-109703677 | Common:1; Rare:88 | ||||
| chr4:109801964-109802249 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr4:109815458-109815538 | Rare:23 | ||||
| chr4:112231494-112231852 | Common:2; Rare:115 | ||||
| chr4:112232129-112232276 | Common:1; Rare:62 | ||||
| chr4:112285738-112285978 | Rare:76 | ||||
| chr4:112636885-112637187 | Common:1; Rare:84 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 |