Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73950189-73950333 | Common:3; Rare:64; Clinvar (benign):1 | ||||
chr14:74019259-74019417 | Common:1; Rare:62 | ||||
chr14:74493565-74493773 | Common:3; Rare:78; Clinvar (benign):4 | ||||
chr14:74713077-74713205 | Rare:62 | ||||
chr14:75126984-75127110 | Rare:43 | ||||
chr14:75278799-75279126 | Common:2; Rare:99 | ||||
chr14:75280527-75280547 | Rare:4 | ||||
chr14:75522360-75522514 | Rare:31 | ||||
chr14:75660862-75661561 | Common:7; Rare:174 | ||||
chr14:77320816-77321060 | Rare:74; Clinvar:3 | ||||
chr14:77377049-77377436 | Common:2; Rare:120 | ||||
chr14:77457545-77457829 | Common:1; Rare:91 | ||||
chr14:77458003-77458131 | Rare:35 | ||||
chr14:77708000-77708149 | Common:2; Rare:80 | ||||
chr14:87993119-87993274 | Common:2; Rare:69; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):2 |