| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75514643-75514796 | Rare:99 | ||||
| chr4:75514781-75515181 | Rare:60 | ||||
| chr4:75672341-75673036 | Common:2; Rare:386 | ||||
| chr4:75673063-75673170 | Rare:26 | ||||
| chr4:75673219-75673781 | Common:7; Rare:1080 | ||||
| chr4:75673928-75674476 | Common:2; Rare:144 | ||||
| chr4:75724320-75724797 | Common:10; Rare:743 | ||||
| chr4:75724831-75725433 | Common:4; Rare:412 | ||||
| chr4:75939834-75939999 | Common:2; Rare:51 | ||||
| chr4:75940170-75940660 | Common:4; Rare:187 | ||||
| chr4:75940952-75941156 | Common:6; Rare:96 | ||||
| chr4:75990840-75991110 | Common:7; Rare:255 | ||||
| chr4:76147643-76148098 | Common:29; Rare:565 | ||||
| chr4:76148226-76149009 | Common:35; Rare:636 | ||||
| chr4:76213400-76214151 | Common:17; Rare:718; Clinvar:3; Clinvar (benign):12 |