| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30686601-30686798 | Common:2; Rare:38 | ||||
| chr6:30717261-30717435 | Common:1; Rare:36 | ||||
| chr6:30720124-30720551 | Common:1; Rare:99 | ||||
| chr6:30742480-30742979 | Common:3; Rare:117 | ||||
| chr6:30882780-30882977 | Common:2; Rare:22 | ||||
| chr6:30914000-30914387 | Common:2; Rare:120; Clinvar (benign):2 | ||||
| chr6:31158171-31158597 | Common:8; Rare:108 | ||||
| chr6:31271939-31272197 | Common:20; Rare:63 | ||||
| chr6:31357084-31357398 | Common:31; Rare:57 | ||||
| chr6:31399739-31400073 | Common:7; Rare:60 | ||||
| chr6:31541921-31542330 | Common:8; Rare:106 | ||||
| chr6:31546579-31546941 | Common:3; Rare:67 | ||||
| chr6:31547428-31547740 | Common:2; Rare:82 | ||||
| chr6:31586913-31587281 | Common:1; Rare:46 | ||||
| chr6:31615538-31615723 | Rare:48 |