| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121870390-121870652 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr4:122152228-122152404 | Common:2; Rare:81 | ||||
| chr4:122732432-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122826479-122826664 | Common:1; Rare:63 | ||||
| chr4:122922566-122922689 | Common:1; Rare:52 | ||||
| chr4:122922951-122923156 | Common:2; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:127632755-127632968 | Common:1; Rare:51 | ||||
| chr4:127880759-127880965 | Rare:75 | ||||
| chr4:127881153-127881421 | Common:1; Rare:88 | ||||
| chr4:128060994-128061384 | Common:1; Rare:133 | ||||
| chr4:128287392-128287425 | Rare:5 | ||||
| chr4:128287805-128287997 | Common:3; Rare:72 | ||||
| chr4:128810901-128811012 | Common:1; Rare:22 | ||||
| chr4:128811037-128811351 | Rare:68 | ||||
| chr4:129093458-129093731 | Common:1; Rare:80 |