chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104531550145315502AG16GENIChomozygous116583351
104531564345315644AT19GENIChomozygous116583353
104531567445315675TC26GENIChomozygous117078064
104531663145316632TC22GENIChomozygous116583355
104531684045316841GA20GENIChomozygous117078065
104531782945317830TC28GENIChomozygous116583359
104531833445318335GC24GENIChomozygous117078066
104531945245319453AG15GENIChomozygous117078067
104531948845319489GA17GENIChomozygous117078068
104531966145319662TA19GENIChomozygous117078069
104531977645319777CT17GENIChomozygous117078070
104532037945320380AG18GENIChomozygous117078071
104532044645320447CT21GENIChomozygous117078072
104532133945321340TC30GENIChomozygous117078073
104532138445321385TC38GENIChomozygous117078074
104532138545321386CT40GENIChomozygous117078075
104532139545321396GA40GENIChomozygous117078076
104532142945321430TG38GENIChomozygous117078077