| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100339381-100339530 | Rare:21 | ||||
| chr10:100373233-100373638 | Common:4; Rare:84 | ||||
| chr10:100374070-100374155 | Rare:20 | ||||
| chr10:101042679-101043006 | Common:1; Rare:60 | ||||
| chr10:101060614-101060882 | Common:2; Rare:64 | ||||
| chr10:101067937-101068145 | Common:1; Rare:56 | ||||
| chr10:101694144-101694299 | Rare:25 | ||||
| chr10:101694327-101694576 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101779218-101779291 | Rare:22 | ||||
| chr10:101814701-101815024 | Common:1; Rare:65 | ||||
| chr10:101840760-101840903 | Rare:31 | ||||
| chr10:101858882-101859016 | Rare:21 | ||||
| chr10:101903912-101904184 | Rare:36 | ||||
| chr10:102117206-102117486 | Rare:45 | ||||
| chr10:102117880-102118035 | Common:1; Rare:33 |