| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52284709-52285092 | Common:2; Rare:125 | ||||
| chr6:52420125-52420392 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995259-52995819 | Common:4; Rare:229 | ||||
| chr6:53061659-53061944 | Rare:63 | ||||
| chr6:53065565-53065598 | Rare:10 | ||||
| chr6:53348878-53349093 | Common:2; Rare:92 | ||||
| chr6:53349146-53349211 | Rare:16 | ||||
| chr6:54846484-54846799 | Common:2; Rare:78 | ||||
| chr6:56542726-56543065 | Common:2; Rare:59 | ||||
| chr6:57172492-57172757 | Common:1; Rare:82 | ||||
| chr6:57221431-57221590 | Rare:34 | ||||
| chr6:57222248-57222373 | Rare:54 | ||||
| chr6:57317586-57317667 | Rare:27 | ||||
| chr6:63572265-63572485 | Rare:85 | ||||
| chr6:68634955-68635382 | Common:2; Rare:116 |