| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17229898-17230053 | Rare:60 | ||||
| chr10:17643871-17644269 | Common:2; Rare:120 | ||||
| chr10:18659227-18659512 | Common:2; Rare:98 | ||||
| chr10:18659760-18659984 | Common:2; Rare:60 | ||||
| chr10:26438060-26438370 | Common:2; Rare:72 | ||||
| chr10:26860790-26861040 | Common:2; Rare:85 | ||||
| chr10:27154212-27154539 | Rare:94 | ||||
| chr10:27155116-27155426 | Common:7; Rare:119; Clinvar:5; Clinvar (benign):7 | ||||
| chr10:27504044-27504367 | Rare:148; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:28334374-28334604 | Common:1; Rare:44 | ||||
| chr10:28532622-28532806 | Common:1; Rare:76 | ||||
| chr10:28533002-28533194 | Rare:76 | ||||
| chr10:30433805-30434387 | Common:4; Rare:169 | ||||
| chr10:30434595-30434766 | Common:1; Rare:50 | ||||
| chr10:31031850-31032052 | Common:2; Rare:82 |