| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116253768-116254225 | Common:11; Rare:157 | ||||
| chr6:116279099-116279615 | Common:4; Rare:196 | ||||
| chr6:116279619-116279963 | Common:2; Rare:136 | ||||
| chr6:116571209-116571593 | Common:3; Rare:108 | ||||
| chr6:117602131-117602252 | Rare:42 | ||||
| chr6:117602372-117602670 | Common:4; Rare:79 | ||||
| chr6:117675318-117675505 | Common:3; Rare:50 | ||||
| chr6:118894075-118894302 | Common:1; Rare:56 | ||||
| chr6:119349732-119349920 | Common:2; Rare:63 | ||||
| chr6:121334454-121334616 | Common:4; Rare:60 | ||||
| chr6:121334698-121334779 | Common:1; Rare:13 | ||||
| chr6:121435497-121435831 | Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122399351-122399752 | Common:6; Rare:151 | ||||
| chr6:122471706-122471937 | Common:3; Rare:80 | ||||
| chr6:122789047-122789457 | Common:2; Rare:115 |