| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97498694-97499138 | Common:2; Rare:129 | ||||
| chr10:97589584-97589773 | Common:1; Rare:41 | ||||
| chr10:97633431-97633606 | Common:2; Rare:43 | ||||
| chr10:97687155-97687507 | Common:6; Rare:107 | ||||
| chr10:97736939-97737212 | Common:2; Rare:93 | ||||
| chr10:98134552-98134946 | Common:3; Rare:129 | ||||
| chr10:98267586-98267832 | Rare:52 | ||||
| chr10:98268188-98268442 | Common:3; Rare:66 | ||||
| chr10:98446263-98446381 | Rare:19 | ||||
| chr10:98446850-98446977 | Rare:37; Clinvar:1 | ||||
| chr10:99329160-99329385 | Common:2; Rare:52 | ||||
| chr10:99430602-99430996 | Common:3; Rare:96 | ||||
| chr10:99620833-99621179 | Common:1; Rare:99 | ||||
| chr10:99659215-99659571 | Common:2; Rare:93 | ||||
| chr10:99732036-99732400 | Rare:136; Clinvar:6; Clinvar (benign):1 |