| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44324770-44325013 | Common:2; Rare:88 | ||||
| chr17:44350506-44350733 | Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44911517-44911571 | Common:2; Rare:15; Clinvar:1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45132298-45132631 | Common:2; Rare:100 | ||||
| chr17:45148152-45148478 | Common:1; Rare:94 | ||||
| chr17:45161530-45161856 | Common:1; Rare:72 | ||||
| chr17:45490708-45490871 | Rare:55 | ||||
| chr17:46923027-46923219 | Common:3; Rare:77; Clinvar:4; Clinvar (benign):9 | ||||
| chr17:47208960-47209568 | Rare:135; Clinvar:2 | ||||
| chr17:47323894-47323962 | Rare:21 | ||||
| chr17:47831516-47831684 | Rare:48 | ||||
| chr17:47841031-47841297 | Rare:61 | ||||
| chr17:47941354-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 |