| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30717261-30717435 | Common:1; Rare:36 | ||||
| chr6:30720124-30720436 | Common:1; Rare:80 | ||||
| chr6:30742466-30742971 | Common:3; Rare:118 | ||||
| chr6:30744160-30744444 | Rare:72 | ||||
| chr6:30744491-30744706 | Common:3; Rare:58 | ||||
| chr6:30907917-30908244 | Common:4; Rare:77 | ||||
| chr6:30914146-30914377 | Rare:84; Clinvar (benign):2 | ||||
| chr6:31158165-31158616 | Common:8; Rare:113 | ||||
| chr6:31272039-31272234 | Common:12; Rare:40 | ||||
| chr6:31357096-31357376 | Common:27; Rare:52 | ||||
| chr6:31399739-31400046 | Common:6; Rare:54 | ||||
| chr6:31497962-31498108 | Common:6; Rare:24 | ||||
| chr6:31541915-31542404 | Common:8; Rare:137 | ||||
| chr6:31547428-31547735 | Common:2; Rare:80 | ||||
| chr6:31620337-31620813 | Common:1; Rare:151 |