| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124092678-124092853 | Common:1; Rare:40 | ||||
| chr10:124092986-124093272 | Common:3; Rare:68 | ||||
| chr10:124093288-124093325 | Rare:8 | ||||
| chr10:124093425-124093846 | Common:3; Rare:78 | ||||
| chr10:124418836-124419114 | Common:6; Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:124450134-124450173 | Rare:13 | ||||
| chr10:124461658-124461962 | Common:6; Rare:89 | ||||
| chr10:124462003-124462332 | Common:4; Rare:98 | ||||
| chr10:124742650-124743014 | Common:1; Rare:67 | ||||
| chr10:124743294-124743371 | Rare:10 | ||||
| chr10:124743737-124744082 | Rare:87 | ||||
| chr10:124744227-124744512 | Common:2; Rare:110 | ||||
| chr10:124744538-124744607 | Rare:22 | ||||
| chr10:124744617-124744732 | Rare:27 | ||||
| chr10:124791707-124792002 | Common:2; Rare:151 |