| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:66697799-66698135 | Common:1; Rare:52 | ||||
| chr17:66700829-66700940 | Rare:21 | ||||
| chr17:66793882-66794113 | Rare:24 | ||||
| chr17:67364186-67364252 | Common:2; Rare:5 | ||||
| chr17:67393326-67393409 | Common:1; Rare:11 | ||||
| chr17:67441231-67441468 | Common:2; Rare:61 | ||||
| chr17:68101486-68101650 | Common:4; Rare:78 | ||||
| chr17:68524876-68524959 | Rare:20; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:72122911-72123081 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73203047-73203292 | Rare:67 | ||||
| chr17:74209006-74209080 | Common:1; Rare:18 | ||||
| chr17:74862786-74863193 | Common:3; Rare:132; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:74982306-74982416 | Common:1; Rare:29 | ||||
| chr17:75243167-75243466 | Common:1; Rare:98 | ||||
| chr17:76050431-76050615 | Common:1; Rare:43 |