| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:127880781-127880934 | Rare:51 | ||||
| chr4:128061010-128061371 | Common:1; Rare:129 | ||||
| chr4:139301223-139301567 | Common:4; Rare:102 | ||||
| chr4:139453680-139453829 | Common:2; Rare:46; Clinvar:1 | ||||
| chr4:139454008-139454204 | Common:2; Rare:55; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:139666053-139666073 | Rare:7 | ||||
| chr4:140153168-140153488 | Common:1; Rare:89 | ||||
| chr4:140154080-140154372 | Common:1; Rare:106 | ||||
| chr4:140373354-140373696 | Common:2; Rare:134 | ||||
| chr4:142846224-142846376 | Rare:36 | ||||
| chr4:143184853-143184949 | Common:5; Rare:36 | ||||
| chr4:145098138-145098356 | Rare:75 | ||||
| chr4:145619237-145619442 | Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145938479-145938906 | Common:2; Rare:76 | ||||
| chr4:147617243-147617463 | Common:1; Rare:50 |