| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151232396-151232525 | Rare:41 | ||||
| chr7:151341555-151341864 | Common:4; Rare:96 | ||||
| chr7:151408935-151409292 | Common:2; Rare:91 | ||||
| chr7:151519134-151519493 | Common:2; Rare:90 | ||||
| chr7:151632573-151632596 | Rare:11 | ||||
| chr7:151877095-151877663 | Common:4; Rare:148; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152025560-152025802 | Common:1; Rare:96 | ||||
| chr7:155644339-155644909 | Common:6; Rare:182 | ||||
| chr7:156640535-156640800 | Common:3; Rare:123 | ||||
| chr7:157138692-157138942 | Common:1; Rare:67 | ||||
| chr7:157336749-157337113 | Common:3; Rare:173; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704774-158704975 | Common:1; Rare:71 | ||||
| chr7:158856423-158856680 | Common:6; Rare:93 | ||||
| chr7:159144834-159145095 | Common:11; Rare:51 | ||||
| chr8:232133-232482 | Common:3; Rare:147 |