| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801243-121801438 | Common:2; Rare:65 | ||||
| chr4:122732433-122732809 | Common:2; Rare:117; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922897-122923139 | Common:2; Rare:68 | ||||
| chr4:127880736-127880924 | Common:1; Rare:72 | ||||
| chr4:128287438-128287599 | Common:1; Rare:60 | ||||
| chr4:129093458-129093723 | Common:1; Rare:78 | ||||
| chr4:133149105-133149309 | Common:2; Rare:60 | ||||
| chr4:137531836-137532043 | Rare:60 | ||||
| chr4:138241807-138241935 | Rare:39 | ||||
| chr4:138242217-138242480 | Common:1; Rare:58 | ||||
| chr4:139084177-139084437 | Common:2; Rare:105 | ||||
| chr4:139280084-139280285 | Common:1; Rare:65 | ||||
| chr4:139301208-139301584 | Common:6; Rare:111 | ||||
| chr4:139302454-139302570 | Common:1; Rare:21 | ||||
| chr4:139453707-139454204 | Common:4; Rare:134; Clinvar:10; Clinvar (benign):4 |