| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24980100-24980478 | Common:10; Rare:146 | ||||
| chr7:24981822-24981938 | Rare:21 | ||||
| chr7:25125175-25125643 | Rare:183; Clinvar:3 | ||||
| chr7:26200564-26200941 | Common:1; Rare:181 | ||||
| chr7:26200990-26201271 | Common:1; Rare:116 | ||||
| chr7:26201396-26201555 | Rare:58 | ||||
| chr7:26201574-26201821 | Common:2; Rare:129 | ||||
| chr7:26864421-26864840 | Common:3; Rare:120 | ||||
| chr7:27095974-27096268 | Rare:76 | ||||
| chr7:27740047-27740223 | Common:5; Rare:56 | ||||
| chr7:28958299-28958545 | Rare:66 | ||||
| chr7:30026391-30026704 | Rare:94; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:30504691-30505090 | Common:4; Rare:135 | ||||
| chr7:30594715-30594959 | Common:4; Rare:112; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:32070785-32071185 | Common:5; Rare:96 |