| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121696885-121697055 | Common:4; Rare:46 | ||||
| chr4:122152225-122152451 | Common:2; Rare:94 | ||||
| chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922982-122923151 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123398079-123398512 | Common:2; Rare:134 | ||||
| chr4:127782255-127782439 | Rare:59 | ||||
| chr4:127880784-127880939 | Rare:52 | ||||
| chr4:128287779-128288057 | Common:3; Rare:106 | ||||
| chr4:128288208-128288480 | Common:5; Rare:85 | ||||
| chr4:128288797-128288907 | Rare:27 | ||||
| chr4:129093494-129093736 | Rare:73 | ||||
| chr4:139177158-139177432 | Rare:77 | ||||
| chr4:139301291-139301562 | Common:4; Rare:84 | ||||
| chr4:139301914-139302120 | Common:3; Rare:49 | ||||
| chr4:139302436-139302478 | Rare:17 |