| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30883599-30883999 | Common:3; Rare:64 | ||||
| chr6:30884283-30884683 | Common:3; Rare:102 | ||||
| chr6:30884832-30884981 | Common:3; Rare:30 | ||||
| chr6:30885808-30886081 | Common:3; Rare:43 | ||||
| chr6:30886432-30886695 | Rare:42 | ||||
| chr6:30907893-30908231 | Common:3; Rare:81 | ||||
| chr6:30914167-30914388 | Rare:76; Clinvar (benign):2 | ||||
| chr6:31158128-31158328 | Common:4; Rare:51 | ||||
| chr6:31271990-31272330 | Common:27; Rare:60 | ||||
| chr6:31357039-31357439 | Common:51; Rare:97 | ||||
| chr6:31403376-31403623 | Common:4; Rare:53 | ||||
| chr6:31541114-31541376 | Common:3; Rare:68 | ||||
| chr6:31541949-31542429 | Common:8; Rare:141 | ||||
| chr6:31546729-31546951 | Common:1; Rare:35 | ||||
| chr6:31547421-31547639 | Common:2; Rare:42 |