| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50087977-50088272 | Common:4; Rare:76; Clinvar:1 | ||||
| chr17:50186315-50186916 | Common:2; Rare:165; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188740-50189011 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50192825-50193004 | Common:2; Rare:57; Clinvar (benign):4 | ||||
| chr17:50195432-50195598 | Rare:35; Clinvar (benign):2 | ||||
| chr17:50195929-50196156 | Common:2; Rare:59; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50373171-50373235 | Common:2; Rare:26 | ||||
| chr17:50719407-50719667 | Common:1; Rare:106 | ||||
| chr17:50866351-50866636 | Common:3; Rare:84 | ||||
| chr17:51260362-51260583 | Common:3; Rare:101 | ||||
| chr17:54968619-54968793 | Common:3; Rare:85 | ||||
| chr17:55722732-55722962 | Common:1; Rare:51 | ||||
| chr17:56914021-56914173 | Rare:38 | ||||
| chr17:57084959-57085105 | Common:1; Rare:49 | ||||
| chr17:57850013-57850274 | Common:1; Rare:80 |