| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148147-45148476 | Common:1; Rare:92 | ||||
| chr17:45490719-45490905 | Rare:62 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189202-47189360 | Common:1; Rare:49 | ||||
| chr17:47208997-47209447 | Rare:83; Clinvar:1 | ||||
| chr17:47831513-47831597 | Rare:26 | ||||
| chr17:47941356-47941600 | Rare:50; Clinvar:1 | ||||
| chr17:48048045-48048397 | Common:1; Rare:95 | ||||
| chr17:48892471-48892836 | Common:3; Rare:89 | ||||
| chr17:49210591-49210711 | Rare:19 | ||||
| chr17:49230698-49230885 | Common:3; Rare:51 | ||||
| chr17:49788576-49788742 | Common:1; Rare:52 | ||||
| chr17:50188740-50189017 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50191382-50191887 | Common:2; Rare:120; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 |