| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30914160-30914370 | Rare:76; Clinvar (benign):2 | ||||
| chr6:31158169-31158530 | Common:8; Rare:84 | ||||
| chr6:31271982-31272241 | Common:19; Rare:55 | ||||
| chr6:31355105-31355585 | Common:27; Rare:142 | ||||
| chr6:31399742-31399794 | Rare:11 | ||||
| chr6:31542036-31542345 | Common:7; Rare:65 | ||||
| chr6:31546567-31546860 | Common:3; Rare:60 | ||||
| chr6:31547428-31547644 | Common:2; Rare:42 | ||||
| chr6:31625808-31626153 | Rare:107 | ||||
| chr6:31651963-31652085 | Rare:30 | ||||
| chr6:31652283-31652415 | Common:7; Rare:40 | ||||
| chr6:31664886-31665266 | Common:4; Rare:95 | ||||
| chr6:31665854-31666182 | Common:4; Rare:90 | ||||
| chr6:31703285-31703414 | Rare:42 | ||||
| chr6:31736285-31736641 | Common:3; Rare:80 |