| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30744255-30744444 | Rare:47 | ||||
| chr6:30744541-30744680 | Common:1; Rare:34 | ||||
| chr6:30914010-30914370 | Common:2; Rare:112; Clinvar (benign):2 | ||||
| chr6:31158171-31158679 | Common:9; Rare:120 | ||||
| chr6:31271994-31272221 | Common:13; Rare:52 | ||||
| chr6:31357146-31357384 | Common:22; Rare:30 | ||||
| chr6:31399742-31399753 | Rare:1 | ||||
| chr6:31399933-31400084 | Common:4; Rare:33 | ||||
| chr6:31541938-31542349 | Common:8; Rare:109 | ||||
| chr6:31542432-31542526 | Rare:28 | ||||
| chr6:31546579-31546893 | Common:3; Rare:58 | ||||
| chr6:31547395-31547644 | Common:2; Rare:45 | ||||
| chr6:31620335-31620808 | Common:1; Rare:150 | ||||
| chr6:31625815-31626162 | Rare:104 | ||||
| chr6:31651973-31652085 | Rare:28 |