| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15860469-15860583 | Rare:33 | ||||
| chr10:31319063-31319240 | Common:2; Rare:54 | ||||
| chr10:31928798-31928926 | Common:1; Rare:47 | ||||
| chr10:32958149-32958502 | Common:2; Rare:136 | ||||
| chr10:42782550-42782809 | Rare:71 | ||||
| chr10:44959552-44959844 | Common:2; Rare:87 | ||||
| chr10:44978807-44979061 | Common:5; Rare:61 | ||||
| chr10:45000909-45000953 | Rare:17 | ||||
| chr10:45972392-45972521 | Rare:31 | ||||
| chr10:50067852-50067977 | Common:2; Rare:56 | ||||
| chr10:52314023-52314300 | Common:1; Rare:64 | ||||
| chr10:73167970-73168133 | Rare:40 | ||||
| chr10:73252575-73252759 | Common:2; Rare:55; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:74176631-74176770 | Rare:38; Clinvar:2 | ||||
| chr10:87504832-87504912 | Common:1; Rare:36 |