| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122732408-122732762 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922510-122922685 | Common:3; Rare:85 | ||||
| chr4:122922896-122923182 | Common:2; Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396667-123396824 | Rare:38 | ||||
| chr4:123399365-123399653 | Common:1; Rare:89 | ||||
| chr4:124712622-124713039 | Common:1; Rare:124 | ||||
| chr4:127632884-127632980 | Rare:22 | ||||
| chr4:127880736-127880939 | Common:1; Rare:74 | ||||
| chr4:128060979-128061329 | Common:1; Rare:125 | ||||
| chr4:128809577-128809825 | Common:1; Rare:73 | ||||
| chr4:129093452-129093731 | Common:1; Rare:80 | ||||
| chr4:137532456-137532689 | Common:1; Rare:36 | ||||
| chr4:139280146-139280341 | Rare:50 | ||||
| chr4:139301197-139301593 | Common:6; Rare:114 | ||||
| chr4:139453939-139454190 | Common:3; Rare:73; Clinvar:6; Clinvar (benign):4 |