| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118893909-118894103 | Common:2; Rare:70 | ||||
| chr6:118894109-118894292 | Common:1; Rare:44 | ||||
| chr6:119349699-119349936 | Common:3; Rare:83 | ||||
| chr6:121334437-121334779 | Common:7; Rare:100 | ||||
| chr6:121435497-121435825 | Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122471701-122471929 | Common:3; Rare:76 | ||||
| chr6:124963016-124963282 | Common:1; Rare:91 | ||||
| chr6:124963523-124963558 | Rare:7 | ||||
| chr6:125749413-125749760 | Common:5; Rare:138 | ||||
| chr6:125781047-125781182 | Rare:24 | ||||
| chr6:125790926-125791044 | Common:2; Rare:26 | ||||
| chr6:125986396-125986571 | Rare:67 | ||||
| chr6:127118945-127119331 | Rare:111 | ||||
| chr6:127119752-127119927 | Rare:45 | ||||
| chr6:127266803-127266920 | Common:1; Rare:45 |