| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148130-45148476 | Common:1; Rare:96 | ||||
| chr17:45160875-45161082 | Rare:69 | ||||
| chr17:45161473-45161921 | Common:1; Rare:120 | ||||
| chr17:45317008-45317334 | Common:4; Rare:82 | ||||
| chr17:45490688-45490914 | Common:3; Rare:73 | ||||
| chr17:45620232-45620369 | Rare:32 | ||||
| chr17:45894208-45894629 | Common:4; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46192775-46193019 | Common:3; Rare:61; Clinvar (benign):2 | ||||
| chr17:46194007-46194270 | Common:5; Rare:44 | ||||
| chr17:46225344-46225466 | Common:1; Rare:33 | ||||
| chr17:46579669-46580002 | Rare:32 | ||||
| chr17:46922827-46923187 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189235-47189574 | Rare:84 | ||||
| chr17:47323894-47324036 | Common:1; Rare:49 | ||||
| chr17:47649324-47649965 | Common:2; Rare:217 |