| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:170090216-170090325 | Common:1; Rare:36 | ||||
| chr4:173369735-173369941 | Common:1; Rare:66 | ||||
| chr4:173370668-173370968 | Common:2; Rare:76 | ||||
| chr4:173530150-173530478 | Common:2; Rare:72 | ||||
| chr4:174283612-174283965 | Common:1; Rare:71 | ||||
| chr4:174522398-174522613 | Rare:70; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:174829213-174829412 | Common:1; Rare:42 | ||||
| chr4:175812189-175812363 | Common:11; Rare:55 | ||||
| chr4:175812369-175812838 | Rare:92 | ||||
| chr4:175813156-175813241 | Common:1; Rare:14 | ||||
| chr4:176002331-176002568 | Rare:67 | ||||
| chr4:176065733-176066031 | Common:7; Rare:95 | ||||
| chr4:176319901-176320042 | Common:2; Rare:63 | ||||
| chr4:177442376-177442523 | Rare:88; Clinvar:2 | ||||
| chr4:182448793-182449068 | Common:2; Rare:97 |