| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50192797-50193049 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194563-50194851 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr17:50195045-50195669 | Common:1; Rare:175; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50196153-50196368 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:50196450-50196672 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:50197940-50198217 | Common:3; Rare:71; Clinvar (benign):7 | ||||
| chr17:50345833-50346143 | Common:4; Rare:94 | ||||
| chr17:50373168-50373304 | Common:4; Rare:51 | ||||
| chr17:50866351-50866568 | Common:2; Rare:68 | ||||
| chr17:51260372-51260589 | Common:3; Rare:102 | ||||
| chr17:54968623-54968792 | Common:3; Rare:82 | ||||
| chr17:56914083-56914174 | Rare:17 | ||||
| chr17:57084992-57085096 | Rare:39 | ||||
| chr17:57850008-57850274 | Common:1; Rare:84 | ||||
| chr17:58692566-58692606 | Rare:20; Clinvar (benign):4 |