| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:129096092-129096170 | Common:1; Rare:18 | ||||
| chr4:133149099-133149295 | Common:2; Rare:57 | ||||
| chr4:137532424-137532826 | Common:2; Rare:74 | ||||
| chr4:138242281-138242646 | Common:1; Rare:79 | ||||
| chr4:139084187-139084538 | Common:4; Rare:156 | ||||
| chr4:139301269-139301824 | Common:5; Rare:165 | ||||
| chr4:139302460-139302604 | Common:1; Rare:25 | ||||
| chr4:139453784-139454337 | Common:3; Rare:165; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr4:140373390-140373701 | Common:2; Rare:128 | ||||
| chr4:141220793-141220978 | Rare:64 | ||||
| chr4:141636318-141636583 | Common:3; Rare:54 | ||||
| chr4:143184685-143184997 | Common:8; Rare:121 | ||||
| chr4:143337088-143337195 | Rare:43 | ||||
| chr4:143513325-143513814 | Common:3; Rare:164 | ||||
| chr4:143513817-143514101 | Common:2; Rare:120 |