| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141636415-141636593 | Common:2; Rare:34 | ||||
| chr4:141636866-141636901 | Rare:5 | ||||
| chr4:142405389-142405446 | Rare:8 | ||||
| chr4:143184793-143184960 | Common:8; Rare:75 | ||||
| chr4:145098141-145098350 | Rare:73 | ||||
| chr4:145619330-145619396 | Rare:25 | ||||
| chr4:147617242-147617432 | Common:1; Rare:41 | ||||
| chr4:147684106-147684289 | Common:1; Rare:71 | ||||
| chr4:151099508-151099713 | Common:3; Rare:86 | ||||
| chr4:152679935-152680112 | Rare:41 | ||||
| chr4:152779790-152780013 | Common:1; Rare:60 | ||||
| chr4:153344508-153344729 | Common:4; Rare:64 | ||||
| chr4:154550372-154550519 | Rare:44 | ||||
| chr4:156971117-156971189 | Rare:9 | ||||
| chr4:158671843-158672359 | Common:5; Rare:126; Clinvar:2; Clinvar (benign):1 |