| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691141-109691319 | Common:3; Rare:44; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:111483088-111483591 | Common:1; Rare:177 | ||||
| chr6:112087467-112087712 | Rare:63 | ||||
| chr6:113857218-113857441 | Common:1; Rare:57 | ||||
| chr6:116100713-116100886 | Rare:64 | ||||
| chr6:116254062-116254175 | Common:1; Rare:26 | ||||
| chr6:116279877-116280064 | Common:1; Rare:63 | ||||
| chr6:116571202-116571598 | Common:3; Rare:113 | ||||
| chr6:119349703-119349921 | Common:2; Rare:71 | ||||
| chr6:122789491-122789801 | Common:1; Rare:79 | ||||
| chr6:127266787-127266924 | Common:1; Rare:58 | ||||
| chr6:127343323-127343394 | Rare:15 | ||||
| chr6:127343472-127343838 | Common:2; Rare:72 | ||||
| chr6:128520571-128520757 | Rare:73 | ||||
| chr6:132401473-132401584 | Common:1; Rare:33 |