| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89638725-89638883 | Common:3; Rare:55 | ||||
| chr6:96521700-96521857 | Common:5; Rare:68 | ||||
| chr6:96897812-96898040 | Common:4; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:99425256-99425623 | Common:2; Rare:90 | ||||
| chr6:100881249-100881485 | Common:5; Rare:94 | ||||
| chr6:105179875-105180062 | Common:4; Rare:53 | ||||
| chr6:106629458-106629649 | Common:3; Rare:46 | ||||
| chr6:109382391-109382806 | Common:5; Rare:135; Clinvar (benign):1 | ||||
| chr6:109440608-109440906 | Common:2; Rare:99 | ||||
| chr6:109691068-109691328 | Common:4; Rare:66; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:111483133-111483597 | Common:1; Rare:165 | ||||
| chr6:112087463-112087704 | Rare:63 | ||||
| chr6:113857213-113857441 | Common:1; Rare:57 | ||||
| chr6:116100717-116100890 | Rare:63 | ||||
| chr6:116254019-116254175 | Common:2; Rare:46 |