| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153759854-153760094 | Common:2; Rare:53 | ||||
| chr4:154492019-154492146 | Rare:29 | ||||
| chr4:154550357-154550519 | Rare:52 | ||||
| chr4:155208726-155208900 | Rare:36 | ||||
| chr4:155376755-155377029 | Rare:74 | ||||
| chr4:155667269-155667493 | Common:1; Rare:52 | ||||
| chr4:157219833-157220149 | Common:1; Rare:69 | ||||
| chr4:157220487-157221067 | Common:5; Rare:155 | ||||
| chr4:157221574-157221663 | Common:2; Rare:27 | ||||
| chr4:158172986-158173186 | Rare:34 | ||||
| chr4:158210484-158210554 | Common:1; Rare:20 | ||||
| chr4:158671830-158672431 | Common:5; Rare:160; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723142-158723470 | Common:2; Rare:139 | ||||
| chr4:159266846-159266934 | Rare:13 | ||||
| chr4:159267058-159267192 | Rare:21 |