| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75630451-75630692 | Rare:56 | ||||
| chr4:75673051-75673244 | Rare:51 | ||||
| chr4:75673245-75673712 | Common:1; Rare:178 | ||||
| chr4:75724348-75724721 | Common:1; Rare:97 | ||||
| chr4:75990881-75991054 | Common:1; Rare:66 | ||||
| chr4:76148155-76148210 | Rare:11 | ||||
| chr4:76148316-76148594 | Common:5; Rare:82 | ||||
| chr4:76213330-76213441 | Common:2; Rare:35; Clinvar (benign):1 | ||||
| chr4:76213506-76214005 | Common:4; Rare:171; Clinvar:1; Clinvar (benign):7 | ||||
| chr4:76251557-76251744 | Common:1; Rare:44 | ||||
| chr4:76949559-76949906 | Common:2; Rare:116 | ||||
| chr4:77075960-77076162 | Common:4; Rare:93 | ||||
| chr4:77076235-77076482 | Common:3; Rare:108 | ||||
| chr4:77156671-77156939 | Common:2; Rare:77 | ||||
| chr4:77157061-77157425 | Common:6; Rare:144 |