| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122732417-122732708 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr4:122922924-122923137 | Common:2; Rare:62 | ||||
| chr4:127880797-127880934 | Rare:45 | ||||
| chr4:128061002-128061399 | Common:1; Rare:134 | ||||
| chr4:129093458-129093731 | Common:1; Rare:80 | ||||
| chr4:139084186-139084205 | Rare:12 | ||||
| chr4:139084209-139084457 | Common:2; Rare:99 | ||||
| chr4:139301181-139301562 | Common:6; Rare:106 | ||||
| chr4:139452993-139453218 | Common:2; Rare:38 | ||||
| chr4:139453693-139453697 | Common:1 | ||||
| chr4:139453699-139454337 | Common:4; Rare:191; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr4:139556100-139556513 | Rare:90 | ||||
| chr4:140153021-140153230 | Rare:72 | ||||
| chr4:140373349-140373709 | Common:3; Rare:143 | ||||
| chr4:140523929-140524231 | Common:2; Rare:93 |