| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97426047-97426454 | Common:2; Rare:170 | ||||
| chr10:97445928-97446247 | Common:1; Rare:93 | ||||
| chr10:97633431-97633671 | Common:2; Rare:64 | ||||
| chr10:97686869-97687012 | Rare:27 | ||||
| chr10:97687051-97687725 | Common:8; Rare:175 | ||||
| chr10:97713414-97713444 | Rare:6 | ||||
| chr10:97714389-97714542 | Rare:37 | ||||
| chr10:97737010-97737220 | Common:1; Rare:72 | ||||
| chr10:98446856-98447031 | Rare:50 | ||||
| chr10:99430548-99430986 | Common:4; Rare:114 | ||||
| chr10:99659219-99659562 | Common:1; Rare:87 | ||||
| chr10:99732069-99732393 | Rare:122; Clinvar:6; Clinvar (benign):1 | ||||
| chr10:99782499-99782876 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:100185883-100186198 | Rare:115 | ||||
| chr10:100229522-100229668 | Rare:55 |