| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801233-121801439 | Common:2; Rare:71 | ||||
| chr4:121823493-121823525 | Rare:11 | ||||
| chr4:122152263-122152390 | Common:2; Rare:57 | ||||
| chr4:122732436-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922902-122923117 | Common:2; Rare:55 | ||||
| chr4:124712085-124712352 | Common:1; Rare:66 | ||||
| chr4:127632767-127632968 | Common:1; Rare:50 | ||||
| chr4:127880797-127880950 | Rare:50 | ||||
| chr4:128061002-128061362 | Common:1; Rare:130 | ||||
| chr4:129093463-129093744 | Common:1; Rare:82 | ||||
| chr4:138241814-138241858 | Rare:14 | ||||
| chr4:138242250-138242622 | Common:1; Rare:78 | ||||
| chr4:139084192-139084451 | Common:2; Rare:109 | ||||
| chr4:139301299-139301593 | Common:3; Rare:92 | ||||
| chr4:139453683-139453696 | Rare:6 |