| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:155666619-155667029 | Common:10; Rare:78 | ||||
| chr4:156971061-156971279 | Common:1; Rare:36 | ||||
| chr4:158172360-158172582 | Rare:33 | ||||
| chr4:158671830-158672359 | Common:5; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723339-158723439 | Common:2; Rare:48 | ||||
| chr4:159103958-159104132 | Common:1; Rare:64 | ||||
| chr4:163166826-163166983 | Common:2; Rare:56 | ||||
| chr4:165327400-165327728 | Common:2; Rare:93 | ||||
| chr4:165873507-165873695 | Common:2; Rare:37 | ||||
| chr4:168318719-168319108 | Common:3; Rare:64 | ||||
| chr4:168480452-168480747 | Common:1; Rare:51 | ||||
| chr4:169010230-169010459 | Common:1; Rare:68 | ||||
| chr4:169620373-169620697 | Common:2; Rare:115 | ||||
| chr4:169757869-169758074 | Rare:59 | ||||
| chr4:170026325-170026589 | Common:4; Rare:103 |