| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110981954-110982100 | Common:2; Rare:71 | ||||
| chr6:112087428-112087641 | Rare:70 | ||||
| chr6:116100695-116100903 | Common:1; Rare:76 | ||||
| chr6:116254073-116254171 | Common:1; Rare:21 | ||||
| chr6:118893919-118894221 | Common:2; Rare:89 | ||||
| chr6:121435518-121435761 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:122471766-122471917 | Common:2; Rare:46 | ||||
| chr6:125956661-125956784 | Common:1; Rare:43 | ||||
| chr6:125986433-125986548 | Rare:45 | ||||
| chr6:127343343-127343420 | Rare:14 | ||||
| chr6:128520569-128520791 | Common:1; Rare:84 | ||||
| chr6:135497728-135497822 | Common:3; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:136289774-136289997 | Common:1; Rare:93 | ||||
| chr6:138773608-138773809 | Common:3; Rare:88 | ||||
| chr6:143060631-143060919 | Common:9; Rare:103 |