| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116279750-116280038 | Common:1; Rare:104 | ||||
| chr6:116370737-116371004 | Rare:70 | ||||
| chr6:116571175-116571600 | Common:3; Rare:123 | ||||
| chr6:117602131-117602241 | Rare:37 | ||||
| chr6:117602267-117602553 | Common:3; Rare:82 | ||||
| chr6:117675325-117675501 | Common:3; Rare:47 | ||||
| chr6:118548254-118548390 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:118894055-118894302 | Common:1; Rare:61 | ||||
| chr6:119349701-119349940 | Common:3; Rare:83 | ||||
| chr6:121334468-121334779 | Common:7; Rare:80 | ||||
| chr6:122399351-122399708 | Common:6; Rare:135 | ||||
| chr6:122471706-122471937 | Common:3; Rare:80 | ||||
| chr6:122789108-122789331 | Common:1; Rare:55 | ||||
| chr6:124962861-124962979 | Rare:40 | ||||
| chr6:124963016-124963345 | Common:2; Rare:109 |