| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116279872-116280120 | Common:2; Rare:78 | ||||
| chr6:116571187-116571521 | Common:2; Rare:87 | ||||
| chr6:118894290-118894294 | Rare:1 | ||||
| chr6:119349641-119349920 | Common:3; Rare:88 | ||||
| chr6:122789491-122789803 | Common:1; Rare:79 | ||||
| chr6:127266785-127267002 | Common:1; Rare:85 | ||||
| chr6:127343331-127343645 | Common:2; Rare:73 | ||||
| chr6:128520569-128520804 | Common:2; Rare:91 | ||||
| chr6:130365400-130365564 | Common:1; Rare:38 | ||||
| chr6:131628101-131628463 | Common:3; Rare:94 | ||||
| chr6:131951364-131951519 | Rare:36 | ||||
| chr6:132401485-132401579 | Common:1; Rare:31 | ||||
| chr6:134177833-134178090 | Common:1; Rare:42 | ||||
| chr6:135497738-135497831 | Common:3; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:136289779-136289917 | Rare:58 |