| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:121334448-121334543 | Common:2; Rare:41 | ||||
| chr6:121334689-121334792 | Common:1; Rare:17 | ||||
| chr6:122471706-122471921 | Common:2; Rare:73 | ||||
| chr6:122789225-122789331 | Common:1; Rare:34 | ||||
| chr6:124963037-124963288 | Common:1; Rare:85 | ||||
| chr6:125781059-125781156 | Rare:18 | ||||
| chr6:125956661-125956945 | Common:1; Rare:76 | ||||
| chr6:125986417-125986553 | Rare:53 | ||||
| chr6:127266791-127266925 | Common:1; Rare:54 | ||||
| chr6:127343343-127343469 | Rare:21 | ||||
| chr6:127343538-127343645 | Common:1; Rare:30 | ||||
| chr6:128520462-128520774 | Common:3; Rare:98 | ||||
| chr6:131573164-131573239 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:131628116-131628433 | Common:3; Rare:86 | ||||
| chr6:131951370-131951437 | Rare:24 |