| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50191788-50192004 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50192476-50192684 | Common:1; Rare:44; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:50193946-50194828 | Common:5; Rare:247; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
| chr17:50195923-50196202 | Common:2; Rare:74; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr17:50196740-50197131 | Common:3; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:50198137-50198506 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50866351-50866587 | Common:3; Rare:72 | ||||
| chr17:51166702-51166954 | Rare:77 | ||||
| chr17:51260397-51260575 | Common:3; Rare:89 | ||||
| chr17:54968607-54968765 | Common:3; Rare:79 | ||||
| chr17:56914027-56914140 | Rare:29 | ||||
| chr17:58352118-58352290 | Common:1; Rare:73 | ||||
| chr17:59106858-59106966 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:59619976-59620129 | Rare:49 | ||||
| chr17:59707394-59707738 | Common:3; Rare:95; Clinvar (benign):3 |