| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122922896-122923159 | Common:2; Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123399445-123399653 | Rare:65 | ||||
| chr4:127782220-127782356 | Common:2; Rare:42 | ||||
| chr4:127880759-127880947 | Rare:68 | ||||
| chr4:128061002-128061398 | Common:1; Rare:134 | ||||
| chr4:128287789-128287907 | Common:1; Rare:57 | ||||
| chr4:128288196-128288396 | Common:5; Rare:74 | ||||
| chr4:128289043-128289221 | Rare:44 | ||||
| chr4:128811017-128811273 | Rare:45 | ||||
| chr4:129093458-129093741 | Common:1; Rare:83 | ||||
| chr4:139301188-139301557 | Common:6; Rare:104 | ||||
| chr4:139302453-139302552 | Rare:19 | ||||
| chr4:139452912-139453199 | Common:3; Rare:51 | ||||
| chr4:139453665-139454252 | Common:5; Rare:176; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556115-139556518 | Rare:85 |