| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30686596-30686779 | Common:2; Rare:36 | ||||
| chr6:30687150-30687552 | Rare:83 | ||||
| chr6:30690714-30690820 | Common:2; Rare:31 | ||||
| chr6:30717210-30717466 | Common:1; Rare:63 | ||||
| chr6:30720120-30720462 | Common:1; Rare:83 | ||||
| chr6:30742462-30742979 | Common:3; Rare:121 | ||||
| chr6:30907970-30908235 | Common:2; Rare:59 | ||||
| chr6:30914160-30914409 | Rare:82; Clinvar (benign):2 | ||||
| chr6:31158165-31158620 | Common:8; Rare:113 | ||||
| chr6:31272065-31272234 | Common:9; Rare:28 | ||||
| chr6:31399741-31400073 | Common:7; Rare:59 | ||||
| chr6:31494474-31494747 | Common:5; Rare:48 | ||||
| chr6:31497976-31498078 | Common:6; Rare:12 | ||||
| chr6:31541750-31542373 | Common:9; Rare:179 | ||||
| chr6:31546729-31546871 | Common:1; Rare:23 |