| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118894335-118894515 | Rare:41 | ||||
| chr6:121334448-121334531 | Common:2; Rare:33 | ||||
| chr6:121334709-121334876 | Common:2; Rare:41 | ||||
| chr6:121435416-121435830 | Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122471762-122471921 | Common:2; Rare:47 | ||||
| chr6:125301850-125302252 | Common:9; Rare:112 | ||||
| chr6:125749413-125749748 | Common:5; Rare:131 | ||||
| chr6:125781060-125781138 | Rare:14 | ||||
| chr6:125956661-125956881 | Common:1; Rare:64 | ||||
| chr6:125986320-125986553 | Common:1; Rare:79 | ||||
| chr6:127266779-127266916 | Common:1; Rare:57 | ||||
| chr6:127342355-127342562 | Common:1; Rare:36 | ||||
| chr6:127343334-127343685 | Common:2; Rare:77 | ||||
| chr6:128520555-128520791 | Common:1; Rare:87 | ||||
| chr6:129710160-129710281 | Rare:33 |