| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122922963-122923159 | Common:2; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123398294-123398467 | Common:1; Rare:58 | ||||
| chr4:124712750-124713057 | Rare:82 | ||||
| chr4:127880784-127880939 | Rare:52 | ||||
| chr4:127965896-127965923 | Common:1; Rare:3; Clinvar (benign):1 | ||||
| chr4:128061000-128061399 | Common:1; Rare:134 | ||||
| chr4:128287789-128288015 | Common:3; Rare:87 | ||||
| chr4:128288208-128288296 | Common:4; Rare:31 | ||||
| chr4:128811136-128811341 | Rare:46 | ||||
| chr4:129093458-129093743 | Common:1; Rare:83 | ||||
| chr4:133149099-133149316 | Common:2; Rare:64 | ||||
| chr4:139301301-139301557 | Common:3; Rare:79 | ||||
| chr4:139453686-139453749 | Common:2; Rare:19 | ||||
| chr4:139453758-139454337 | Common:3; Rare:172; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr4:139556103-139556569 | Rare:97 |