| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150737283-150737672 | Common:7; Rare:97 | ||||
| chr7:150800310-150800850 | Common:8; Rare:136 | ||||
| chr7:151028128-151028513 | Rare:141 | ||||
| chr7:151057887-151058229 | Common:4; Rare:84 | ||||
| chr7:151059338-151059712 | Common:1; Rare:97 | ||||
| chr7:151080788-151080928 | Rare:41 | ||||
| chr7:151083451-151083777 | Common:1; Rare:73 | ||||
| chr7:151227166-151227429 | Common:1; Rare:70 | ||||
| chr7:151408950-151409284 | Common:2; Rare:86 | ||||
| chr7:151877149-151877509 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152025547-152025775 | Common:1; Rare:93 | ||||
| chr7:152676138-152676275 | Common:2; Rare:50 | ||||
| chr7:155644377-155644724 | Common:2; Rare:120 | ||||
| chr7:156640554-156640737 | Common:2; Rare:90 | ||||
| chr7:157336790-157337070 | Common:2; Rare:129; Clinvar:1 |