| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118651537-118651816 | Common:4; Rare:94 | ||||
| chr6:118893942-118894302 | Common:2; Rare:103 | ||||
| chr6:119349750-119349940 | Common:2; Rare:66 | ||||
| chr6:121334441-121334591 | Common:4; Rare:65 | ||||
| chr6:121334699-121334779 | Common:1; Rare:13 | ||||
| chr6:122399351-122399715 | Common:6; Rare:138 | ||||
| chr6:122471733-122471921 | Common:2; Rare:60 | ||||
| chr6:122789070-122789331 | Common:1; Rare:62 | ||||
| chr6:123636869-123637049 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:124963076-124963264 | Common:1; Rare:66 | ||||
| chr6:125986429-125986548 | Rare:46 | ||||
| chr6:127266798-127266916 | Common:1; Rare:44 | ||||
| chr6:127343344-127343420 | Rare:14 | ||||
| chr6:127343562-127343564 | |||||
| chr6:128520561-128520747 | Rare:69 |