| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:133149105-133149314 | Common:2; Rare:61 | ||||
| chr4:139453774-139454138 | Common:2; Rare:89; Clinvar:9; Clinvar (benign):2 | ||||
| chr4:140373384-140373680 | Common:2; Rare:113 | ||||
| chr4:143336863-143336887 | Rare:9 | ||||
| chr4:143513286-143513750 | Common:3; Rare:152 | ||||
| chr4:145098156-145098322 | Rare:59 | ||||
| chr4:145619350-145619396 | Rare:15 | ||||
| chr4:147617254-147617426 | Common:1; Rare:37 | ||||
| chr4:147684096-147684296 | Common:1; Rare:80 | ||||
| chr4:150581763-150581973 | Rare:44 | ||||
| chr4:151408984-151409188 | Common:3; Rare:65 | ||||
| chr4:152779730-152780009 | Common:1; Rare:78 | ||||
| chr4:153153001-153153140 | Rare:25 | ||||
| chr4:158671830-158672355 | Common:5; Rare:131; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723362-158723433 | Rare:32 |