| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118548113-118548344 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:118893809-118894246 | Common:10; Rare:125 | ||||
| chr6:119349750-119349936 | Common:2; Rare:65 | ||||
| chr6:121334450-121334543 | Common:2; Rare:40 | ||||
| chr6:121334709-121334791 | Common:1; Rare:15 | ||||
| chr6:122471739-122471921 | Common:2; Rare:58 | ||||
| chr6:124962869-124962999 | Rare:44 | ||||
| chr6:124963037-124963278 | Common:1; Rare:82 | ||||
| chr6:125956661-125956971 | Common:1; Rare:89 | ||||
| chr6:125986433-125986548 | Rare:45 | ||||
| chr6:127266787-127266899 | Common:1; Rare:41 | ||||
| chr6:127343346-127343433 | Rare:15 | ||||
| chr6:127343484-127343680 | Common:2; Rare:49 | ||||
| chr6:127459351-127459489 | Common:2; Rare:19 | ||||
| chr6:128520474-128520787 | Common:3; Rare:103 |