| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17229043-17229476 | Common:4; Rare:98 | ||||
| chr10:17643850-17644263 | Common:2; Rare:129 | ||||
| chr10:18651564-18651670 | Common:1; Rare:42 | ||||
| chr10:22316210-22316453 | Common:2; Rare:109 | ||||
| chr10:22325490-22325671 | Common:1; Rare:80 | ||||
| chr10:24449315-24449446 | Rare:20 | ||||
| chr10:27154334-27154426 | Rare:26 | ||||
| chr10:27155197-27155390 | Common:4; Rare:69; Clinvar:3; Clinvar (benign):4 | ||||
| chr10:27242083-27242218 | Common:1; Rare:55 | ||||
| chr10:27504077-27504361 | Rare:138; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:28677260-28677526 | Common:5; Rare:125 | ||||
| chr10:29735775-29735863 | Common:2; Rare:16 | ||||
| chr10:29735909-29735971 | Common:1; Rare:15 | ||||
| chr10:30059503-30059689 | Common:1; Rare:70 | ||||
| chr10:31031850-31032018 | Common:1; Rare:63 |