| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152779721-152780016 | Common:1; Rare:83 | ||||
| chr4:153152191-153152352 | Rare:39 | ||||
| chr4:153152991-153153145 | Rare:28 | ||||
| chr4:153204269-153204463 | Common:1; Rare:38 | ||||
| chr4:153257221-153257496 | Common:1; Rare:48 | ||||
| chr4:154550372-154550498 | Rare:38 | ||||
| chr4:155376781-155377040 | Rare:64 | ||||
| chr4:157220495-157220818 | Common:5; Rare:93 | ||||
| chr4:158671860-158672383 | Common:5; Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723311-158723433 | Common:2; Rare:60 | ||||
| chr4:159267063-159267193 | Rare:19 | ||||
| chr4:159267976-159268192 | Common:1; Rare:59 | ||||
| chr4:162163932-162164316 | Common:1; Rare:83 | ||||
| chr4:163332587-163332669 | Rare:11 | ||||
| chr4:164383393-164383524 | Common:2; Rare:38 |