| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96521543-96521898 | Common:10; Rare:151 | ||||
| chr6:96897821-96898012 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:99424684-99424926 | Rare:64 | ||||
| chr6:99425219-99425425 | Common:1; Rare:62 | ||||
| chr6:100881173-100881498 | Common:6; Rare:118 | ||||
| chr6:106325609-106325906 | Common:1; Rare:105 | ||||
| chr6:106629476-106629614 | Common:1; Rare:25 | ||||
| chr6:107459522-107459690 | Common:1; Rare:38 | ||||
| chr6:108260881-108261134 | Rare:109 | ||||
| chr6:108560726-108560984 | Rare:107 | ||||
| chr6:108848317-108848485 | Rare:62 | ||||
| chr6:109094434-109094579 | Rare:31 | ||||
| chr6:109095384-109095557 | Rare:36 | ||||
| chr6:109382210-109382324 | Rare:51 | ||||
| chr6:109382372-109382838 | Common:6; Rare:153; Clinvar (benign):1 |