| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149873800-149874084 | Common:3; Rare:108 | ||||
| chr7:150379061-150379358 | Common:2; Rare:106 | ||||
| chr7:150450821-150450856 | Rare:14 | ||||
| chr7:150737189-150737464 | Common:3; Rare:53 | ||||
| chr7:150800293-150800820 | Common:7; Rare:135 | ||||
| chr7:151080785-151080979 | Rare:62 | ||||
| chr7:151232415-151232525 | Rare:34 | ||||
| chr7:151471415-151471706 | Common:1; Rare:60 | ||||
| chr7:151632570-151632596 | Rare:11 | ||||
| chr7:151736456-151736616 | Rare:25 | ||||
| chr7:151877149-151877521 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:155644377-155644740 | Common:2; Rare:124 | ||||
| chr7:157139172-157139246 | Common:3; Rare:25 | ||||
| chr7:157336778-157337132 | Common:3; Rare:166; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704800-158705016 | Common:1; Rare:82 |