Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:70600630-70600909 | Common:3; Rare:67 | ||||
chr14:71320300-71320476 | Rare:54 | ||||
chr14:71321015-71321164 | Common:1; Rare:55 | ||||
chr14:73027039-73027351 | Common:2; Rare:86 | ||||
chr14:73058303-73058579 | Common:3; Rare:82 | ||||
chr14:73136361-73136555 | Common:4; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
chr14:73458513-73458870 | Common:5; Rare:94 | ||||
chr14:73787121-73787350 | Common:2; Rare:83 | ||||
chr14:73851750-73851974 | Common:4; Rare:78 | ||||
chr14:73886815-73886903 | Common:1; Rare:30 | ||||
chr14:73950050-73950333 | Common:6; Rare:122; Clinvar (benign):5 | ||||
chr14:74019263-74019436 | Common:1; Rare:68 | ||||
chr14:74493570-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
chr14:74713058-74713207 | Rare:81 | ||||
chr14:74763165-74763397 | Rare:74 |