Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:39583974-39584418 | Common:1; Rare:119 | ||||
chr15:39589354-39589692 | Rare:62 | ||||
chr15:48421587-48421881 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr15:48456638-48456848 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
chr15:51094651-51094834 | Common:5; Rare:46 | ||||
chr15:62657653-62657876 | Rare:48 | ||||
chr15:64594948-64595077 | Common:2; Rare:30 | ||||
chr15:64955011-64955291 | Common:5; Rare:60 | ||||
chr15:66484887-66485115 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):5 | ||||
chr15:71691495-71691792 | Common:1; Rare:48 | ||||
chr15:73927695-73927846 | Common:1; Rare:45 | ||||
chr15:78923021-78923198 | Rare:64 | ||||
chr15:82372616-82372761 | Rare:32 | ||||
chr15:82750411-82750580 | Common:2; Rare:45 | ||||
chr15:84570617-84571139 | Common:6; Rare:135 |