Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67816578-67816705 | Rare:22 | ||||
chr14:68793041-68793183 | Rare:37 | ||||
chr14:68979174-68979514 | Common:2; Rare:96 | ||||
chr14:69398248-69398740 | Common:2; Rare:147 | ||||
chr14:69611456-69611750 | Common:1; Rare:100 | ||||
chr14:69767683-69767967 | Common:1; Rare:121 | ||||
chr14:71320296-71320485 | Rare:59 | ||||
chr14:72894060-72894327 | Common:5; Rare:82 | ||||
chr14:73058309-73058595 | Common:3; Rare:88 | ||||
chr14:73569132-73569286 | Rare:40 | ||||
chr14:73787121-73787475 | Common:2; Rare:115 | ||||
chr14:73790110-73790366 | Common:2; Rare:44 | ||||
chr14:73851733-73851974 | Common:4; Rare:82 | ||||
chr14:73886783-73886893 | Common:2; Rare:36 | ||||
chr14:73950086-73950322 | Common:5; Rare:93; Clinvar (benign):3 |