| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:148698557-148699020 | Common:4; Rare:163 | ||||
| chr7:148884137-148884521 | Common:2; Rare:178; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:149028368-149028938 | Common:7; Rare:204 | ||||
| chr7:149090657-149090908 | Rare:70 | ||||
| chr7:149091269-149091383 | Rare:24 | ||||
| chr7:149126234-149126465 | Common:7; Rare:80 | ||||
| chr7:149147322-149147462 | Common:3; Rare:37 | ||||
| chr7:149148128-149148431 | Common:2; Rare:49 | ||||
| chr7:149239341-149239706 | Common:3; Rare:81 | ||||
| chr7:149261911-149262275 | Common:3; Rare:114 | ||||
| chr7:149714659-149715051 | Common:4; Rare:130 | ||||
| chr7:149838233-149838499 | Rare:67 | ||||
| chr7:149873642-149874047 | Common:5; Rare:137 | ||||
| chr7:150323141-150323375 | Common:6; Rare:66 | ||||
| chr7:150323598-150323668 | Rare:30 |