| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:45373985-45374282 | Common:5; Rare:101 | ||||
| chr10:45594609-45594714 | Rare:32 | ||||
| chr10:45727149-45727315 | Common:1; Rare:71 | ||||
| chr10:45972358-45972564 | Common:1; Rare:66 | ||||
| chr10:46030551-46030725 | Common:1; Rare:59 | ||||
| chr10:48684782-48684904 | Rare:23 | ||||
| chr10:49539023-49539213 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941928-49942091 | Rare:44 | ||||
| chr10:50067817-50067971 | Common:4; Rare:66 | ||||
| chr10:50623891-50624084 | Common:1; Rare:78 | ||||
| chr10:56361193-56361518 | Common:7; Rare:127 | ||||
| chr10:58268863-58269237 | Common:6; Rare:102 | ||||
| chr10:58385277-58385475 | Common:3; Rare:73 | ||||
| chr10:60778257-60778542 | Common:2; Rare:69 | ||||
| chr10:61901175-61901234 | Rare:16 |