| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173370681-173370994 | Common:2; Rare:81 | ||||
| chr4:173371164-173371391 | Common:3; Rare:78 | ||||
| chr4:173530168-173530475 | Common:2; Rare:66 | ||||
| chr4:174283111-174283373 | Rare:40 | ||||
| chr4:174283599-174283965 | Common:1; Rare:73 | ||||
| chr4:174284262-174284320 | Rare:15 | ||||
| chr4:174522429-174522617 | Rare:61; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:176319787-176320055 | Common:3; Rare:101 | ||||
| chr4:177442376-177442519 | Rare:86; Clinvar:2 | ||||
| chr4:182143800-182143982 | Common:2; Rare:44 | ||||
| chr4:182144108-182144227 | Common:4; Rare:37 | ||||
| chr4:182144392-182144731 | Common:4; Rare:108 | ||||
| chr4:182917301-182917558 | Common:4; Rare:83 | ||||
| chr4:183444332-183444782 | Common:2; Rare:195 | ||||
| chr4:183504533-183504817 | Common:3; Rare:88 |