Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67660222-67660337 | Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
chr16:67666700-67666845 | Rare:30 | ||||
chr16:67935698-67935902 | Common:1; Rare:60 | ||||
chr16:67936820-67937158 | Common:1; Rare:60 | ||||
chr16:67966785-67967011 | Rare:46 | ||||
chr16:68023209-68023298 | Common:1; Rare:23 | ||||
chr16:68245163-68245391 | Common:1; Rare:64 | ||||
chr16:68264327-68264681 | Rare:99 | ||||
chr16:68287277-68287565 | Common:1; Rare:62 | ||||
chr16:68287761-68288092 | Common:4; Rare:84 | ||||
chr16:68310915-68311081 | Common:1; Rare:83 | ||||
chr16:69132526-69132663 | Rare:51 | ||||
chr16:69187005-69187156 | Rare:53 | ||||
chr16:69339532-69339822 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):3 | ||||
chr16:69566003-69566284 | Common:2; Rare:84 |