| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:30348474-30348549 | Rare:14 | ||||
| chr10:30349018-30349135 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr10:30349215-30349451 | Common:12; Rare:104 | ||||
| chr10:30433387-30433545 | Common:1; Rare:40 | ||||
| chr10:30433775-30434243 | Common:4; Rare:142 | ||||
| chr10:30434440-30434703 | Common:2; Rare:64 | ||||
| chr10:30434781-30434865 | Rare:15 | ||||
| chr10:31031663-31032132 | Common:3; Rare:164 | ||||
| chr10:31032306-31032616 | Common:13; Rare:98 | ||||
| chr10:31319028-31319273 | Common:2; Rare:71 | ||||
| chr10:31319431-31319468 | Rare:16 | ||||
| chr10:31319474-31319824 | Common:4; Rare:111 | ||||
| chr10:31928296-31928651 | Common:4; Rare:111 | ||||
| chr10:31928727-31928995 | Common:4; Rare:102 | ||||
| chr10:32055871-32056086 | Rare:72 |