| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:123028293-123028499 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:128126644-128126745 | Common:1; Rare:14 | ||||
| chr4:128485818-128485835 | Rare:1 | ||||
| chr4:128570541-128570787 | Common:4; Rare:38 | ||||
| chr4:128869792-128870045 | Common:2; Rare:44 | ||||
| chr4:128970377-128970650 | Common:1; Rare:64 | ||||
| chr4:129069033-129069254 | Common:2; Rare:37 | ||||
| chr4:129071636-129071689 | Rare:10 | ||||
| chr4:138214082-138214343 | Common:4; Rare:48 | ||||
| chr4:138256006-138256211 | Common:1; Rare:33 | ||||
| chr4:139083426-139083651 | Rare:58 | ||||
| chr4:139179027-139179187 | Rare:36 | ||||
| chr4:139703854-139704138 | Common:1; Rare:63 | ||||
| chr4:139861341-139861575 | Common:1; Rare:38 | ||||
| chr4:139861802-139861979 | Common:2; Rare:26 |