| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:42782656-42782811 | Rare:38 | ||||
| chr10:43138410-43138555 | Common:2; Rare:54 | ||||
| chr10:43397209-43397374 | Common:1; Rare:51 | ||||
| chr10:43436819-43437140 | Common:3; Rare:136 | ||||
| chr10:43606370-43606468 | Common:3; Rare:28 | ||||
| chr10:43648816-43649140 | Common:3; Rare:84 | ||||
| chr10:44959574-44959821 | Common:2; Rare:77 | ||||
| chr10:45000773-45000968 | Common:1; Rare:79 | ||||
| chr10:45727134-45727307 | Common:1; Rare:68 | ||||
| chr10:45972345-45972581 | Common:1; Rare:76 | ||||
| chr10:46030549-46030719 | Common:1; Rare:59 | ||||
| chr10:48306546-48306766 | Common:2; Rare:103 | ||||
| chr10:49539023-49539217 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941928-49942118 | Rare:55 | ||||
| chr10:50067857-50068004 | Common:3; Rare:69 |