| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124093062-124093356 | Common:4; Rare:73 | ||||
| chr10:124093471-124093712 | Common:2; Rare:43 | ||||
| chr10:124418881-124419112 | Common:5; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124743249-124743498 | Common:1; Rare:45 | ||||
| chr10:124791728-124791959 | Common:1; Rare:121 | ||||
| chr10:124801735-124801871 | Rare:48 | ||||
| chr10:125138041-125138231 | Rare:42 | ||||
| chr10:125160526-125160757 | Rare:22 | ||||
| chr10:125719433-125719787 | Common:1; Rare:134 | ||||
| chr10:125823085-125823615 | Common:2; Rare:189; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:125896455-125896635 | Common:4; Rare:20 | ||||
| chr10:126905255-126905479 | Rare:89 | ||||
| chr10:128047456-128047696 | Common:4; Rare:83 | ||||
| chr10:131981792-131982134 | Common:4; Rare:119 | ||||
| chr10:132331795-132332269 | Common:16; Rare:161 |