| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:18651543-18651720 | Common:1; Rare:72 | ||||
| chr10:18659226-18659483 | Common:2; Rare:89 | ||||
| chr10:19816281-19816464 | Common:5; Rare:31 | ||||
| chr10:20897125-20897393 | Common:1; Rare:84; Clinvar:5; Clinvar (benign):10 | ||||
| chr10:20897567-20897667 | Rare:20 | ||||
| chr10:21524597-21524662 | Rare:13 | ||||
| chr10:21526355-21526572 | Common:1; Rare:63 | ||||
| chr10:21533955-21534241 | Common:1; Rare:105 | ||||
| chr10:22316292-22316483 | Common:1; Rare:80 | ||||
| chr10:22321358-22321590 | Rare:85 | ||||
| chr10:24208780-24209213 | Common:1; Rare:123 | ||||
| chr10:24722597-24722836 | Rare:61 | ||||
| chr10:24952567-24952874 | Common:4; Rare:92 | ||||
| chr10:25016405-25016608 | Common:6; Rare:62 | ||||
| chr10:27100419-27100582 | Common:3; Rare:50; Clinvar:4; Clinvar (benign):2 |