| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150379075-150379358 | Common:1; Rare:99 | ||||
| chr7:151028214-151028513 | Rare:121 | ||||
| chr7:151057814-151058229 | Common:4; Rare:115 | ||||
| chr7:151062371-151062627 | Common:1; Rare:53 | ||||
| chr7:151080785-151080928 | Rare:41 | ||||
| chr7:151083454-151083606 | Common:1; Rare:34 | ||||
| chr7:151227153-151227509 | Common:2; Rare:89 | ||||
| chr7:151240114-151240456 | Common:5; Rare:92 | ||||
| chr7:151277084-151277268 | Rare:62 | ||||
| chr7:151341626-151341864 | Common:3; Rare:79 | ||||
| chr7:151519565-151519719 | Rare:35 | ||||
| chr7:151632569-151632619 | Rare:21 | ||||
| chr7:151877227-151877535 | Common:1; Rare:84 | ||||
| chr7:152025558-152025802 | Common:1; Rare:96 | ||||
| chr7:152676094-152676328 | Common:2; Rare:106; Clinvar (benign):7 |