| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100997003-100997137 | Rare:39 | ||||
| chr10:100998117-100998324 | Common:1; Rare:47 | ||||
| chr10:100999618-100999936 | Common:2; Rare:93 | ||||
| chr10:101031102-101031496 | Common:1; Rare:91 | ||||
| chr10:101353768-101354219 | Common:1; Rare:138 | ||||
| chr10:101588140-101588357 | Rare:90; Clinvar:1 | ||||
| chr10:101694859-101695166 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101783265-101783492 | Rare:98 | ||||
| chr10:101817955-101818325 | Common:1; Rare:118 | ||||
| chr10:101818334-101819088 | Common:2; Rare:179 | ||||
| chr10:102056089-102056377 | Common:1; Rare:71 | ||||
| chr10:102114938-102115061 | Common:1; Rare:42 | ||||
| chr10:102132835-102133082 | Common:1; Rare:66 | ||||
| chr10:102152281-102152437 | Rare:74 | ||||
| chr10:102226140-102226328 | Common:1; Rare:44 |