| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122349024-122349242 | Common:1; Rare:37 | ||||
| chr4:122732417-122732768 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922935-122923191 | Common:2; Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123399317-123399546 | Common:1; Rare:72 | ||||
| chr4:127880764-127880939 | Rare:62 | ||||
| chr4:127965896-127965928 | Common:1; Rare:4; Clinvar (benign):1 | ||||
| chr4:128061002-128061395 | Common:1; Rare:133 | ||||
| chr4:128287779-128288016 | Common:3; Rare:93 | ||||
| chr4:128288172-128288400 | Common:5; Rare:81 | ||||
| chr4:128811233-128811317 | Rare:20 | ||||
| chr4:129093380-129093741 | Common:2; Rare:100 | ||||
| chr4:129096092-129096175 | Common:1; Rare:19 | ||||
| chr4:139084186-139084464 | Common:3; Rare:119 | ||||
| chr4:139177144-139177437 | Rare:83 | ||||
| chr4:139301168-139301557 | Common:6; Rare:108 |