| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:144355144-144355460 | Rare:3 | ||||
| chr7:144836026-144836198 | Common:2; Rare:65 | ||||
| chr7:149028368-149028938 | Common:7; Rare:204 | ||||
| chr7:149090656-149090887 | Rare:69 | ||||
| chr7:149126248-149126439 | Common:6; Rare:61 | ||||
| chr7:149714664-149714996 | Common:3; Rare:108 | ||||
| chr7:151028149-151028505 | Rare:132 | ||||
| chr7:151057856-151058157 | Common:3; Rare:90 | ||||
| chr7:151059472-151059712 | Common:1; Rare:73 | ||||
| chr7:151080793-151080964 | Rare:52 | ||||
| chr7:151082992-151083182 | Rare:35 | ||||
| chr7:151116166-151116373 | Common:3; Rare:47 | ||||
| chr7:151227162-151227425 | Common:1; Rare:71 | ||||
| chr7:152025583-152025802 | Rare:87 | ||||
| chr7:152676094-152676306 | Common:2; Rare:94; Clinvar (benign):7 |