| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151015718-151015860 | Rare:68 | ||||
| chr4:151099485-151099713 | Common:3; Rare:92 | ||||
| chr4:151408909-151409257 | Common:4; Rare:114 | ||||
| chr4:151760975-151761249 | Common:1; Rare:86 | ||||
| chr4:152536056-152536293 | Rare:90 | ||||
| chr4:152679870-152680065 | Rare:74 | ||||
| chr4:152779730-152780009 | Common:1; Rare:78 | ||||
| chr4:153153043-153153122 | Rare:11 | ||||
| chr4:153204279-153204537 | Common:2; Rare:59 | ||||
| chr4:156774523-156774715 | Common:5; Rare:32 | ||||
| chr4:156970895-156971032 | Rare:24 | ||||
| chr4:156971061-156971215 | Rare:22 | ||||
| chr4:158210282-158210575 | Common:3; Rare:72 | ||||
| chr4:158671843-158672331 | Common:5; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723296-158723488 | Common:2; Rare:87 |