| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110918830-110919050 | Common:1; Rare:63 | ||||
| chr10:110919122-110919690 | Common:23; Rare:408; Clinvar:3; Clinvar (benign):2 | ||||
| chr10:110919843-110920526 | Common:6; Rare:232 | ||||
| chr10:111076660-111077120 | Common:2; Rare:117; Clinvar (benign):1 | ||||
| chr10:112183644-112183893 | Common:7; Rare:197 | ||||
| chr10:112446094-112446586 | Common:8; Rare:148 | ||||
| chr10:112446708-112447465 | Common:10; Rare:442 | ||||
| chr10:112447507-112447631 | Common:2; Rare:44 | ||||
| chr10:112949893-112950406 | Common:9; Rare:277 | ||||
| chr10:113678958-113679312 | Common:3; Rare:93 | ||||
| chr10:113679552-113679977 | Common:13; Rare:341 | ||||
| chr10:113680417-113680734 | Rare:57 | ||||
| chr10:113751389-113751768 | Common:2; Rare:59 | ||||
| chr10:113854143-113854914 | Common:3; Rare:453 | ||||
| chr10:114043380-114043921 | Common:4; Rare:251 |