| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1555492-1555809 | Common:2; Rare:84 | ||||
| chr7:1556177-1556228 | Common:1; Rare:16 | ||||
| chr7:1569950-1570118 | Common:1; Rare:61 | ||||
| chr7:2242162-2242283 | Common:2; Rare:66 | ||||
| chr7:2354047-2354102 | Rare:29 | ||||
| chr7:2354542-2354962 | Common:5; Rare:178 | ||||
| chr7:2354986-2355416 | Common:7; Rare:187 | ||||
| chr7:2403290-2403631 | Common:1; Rare:134 | ||||
| chr7:4682106-4682295 | Rare:70 | ||||
| chr7:4775477-4775691 | Common:6; Rare:102; Clinvar:1 | ||||
| chr7:5190366-5190489 | Common:1; Rare:44 | ||||
| chr7:5527913-5528749 | Common:3; Rare:238; Clinvar:3; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr7:5529801-5530032 | Common:1; Rare:103 | ||||
| chr7:5562697-5562924 | Rare:58 | ||||
| chr7:5592676-5593068 | Common:2; Rare:139 |