| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30686627-30686763 | Common:1; Rare:27 | ||||
| chr6:30717261-30717577 | Common:1; Rare:73 | ||||
| chr6:30720128-30720422 | Common:1; Rare:76 | ||||
| chr6:30742552-30742979 | Common:2; Rare:101 | ||||
| chr6:30744530-30744667 | Common:1; Rare:35 | ||||
| chr6:30883797-30883913 | Common:2; Rare:17 | ||||
| chr6:30885585-30885666 | Rare:10 | ||||
| chr6:30914000-30914370 | Common:2; Rare:117; Clinvar (benign):2 | ||||
| chr6:31145073-31145227 | Common:2; Rare:44 | ||||
| chr6:31158165-31158620 | Common:8; Rare:113 | ||||
| chr6:31271597-31272146 | Common:48; Rare:169 | ||||
| chr6:31355105-31355607 | Common:27; Rare:153 | ||||
| chr6:31357028-31357373 | Common:34; Rare:78 | ||||
| chr6:31399742-31400079 | Common:7; Rare:59 | ||||
| chr6:31541938-31542309 | Common:7; Rare:98 |