| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:133149111-133149294 | Common:2; Rare:52 | ||||
| chr4:137532378-137532704 | Common:2; Rare:55 | ||||
| chr4:138242329-138242646 | Common:1; Rare:67 | ||||
| chr4:139177181-139177411 | Rare:64 | ||||
| chr4:139301291-139301557 | Common:4; Rare:82 | ||||
| chr4:139302463-139302511 | Rare:9 | ||||
| chr4:139386080-139386167 | Rare:22 | ||||
| chr4:139453683-139453697 | Common:1; Rare:6 | ||||
| chr4:139453699-139454204 | Common:4; Rare:136; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556148-139556310 | Rare:38 | ||||
| chr4:139556397-139556633 | Rare:37 | ||||
| chr4:140154068-140154284 | Common:1; Rare:84 | ||||
| chr4:140373384-140373701 | Common:2; Rare:129 | ||||
| chr4:140427576-140427686 | Common:2; Rare:21 | ||||
| chr4:140523929-140524222 | Common:2; Rare:90 |