| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145735225-145735343 | Common:4; Rare:45; Clinvar:10; Clinvar (benign):3 | ||||
| chr6:145735428-145735512 | Rare:16; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:145735999-145736206 | Common:2; Rare:42 | ||||
| chr6:145814662-145814926 | Common:1; Rare:118 | ||||
| chr6:145963991-145964132 | Common:4; Rare:31 | ||||
| chr6:145964272-145964576 | Common:1; Rare:107 | ||||
| chr6:148342433-148342863 | Rare:107 | ||||
| chr6:148746708-148747095 | Common:1; Rare:99 | ||||
| chr6:148747560-148747638 | Rare:31 | ||||
| chr6:149545989-149546141 | Rare:64 | ||||
| chr6:149648552-149648864 | Common:2; Rare:90 | ||||
| chr6:149718049-149718132 | Common:1; Rare:25 | ||||
| chr6:149749693-149749875 | Rare:90 | ||||
| chr6:149864254-149864450 | Common:3; Rare:64 | ||||
| chr6:149963819-149964024 | Common:1; Rare:65 |