| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97426055-97426298 | Common:2; Rare:101 | ||||
| chr10:97445975-97446223 | Rare:66 | ||||
| chr10:97498376-97498544 | Common:2; Rare:71 | ||||
| chr10:97498694-97498947 | Common:2; Rare:73 | ||||
| chr10:97736939-97737173 | Common:2; Rare:80 | ||||
| chr10:98446874-98447053 | Rare:52 | ||||
| chr10:99430621-99430930 | Common:3; Rare:69 | ||||
| chr10:99659239-99659536 | Common:1; Rare:75 | ||||
| chr10:99732072-99732331 | Rare:95; Clinvar:4 | ||||
| chr10:100185920-100186137 | Rare:82 | ||||
| chr10:100229562-100229664 | Rare:33 | ||||
| chr10:100267616-100267746 | Common:2; Rare:40 | ||||
| chr10:100346953-100347283 | Common:1; Rare:78 | ||||
| chr10:100987228-100987593 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101031102-101031275 | Common:1; Rare:41 |