chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73424139134241392AC40GENIChomozygous54725897
73424170734241708CT29GENIChomozygous53869685
73424171134241712TC26GENIChomozygous54725899
73424262734242628AG31GENIChomozygous54725901
73424269334242694AG37GENIChomozygous54725903
73424326334243264GGGAGAGGGAGA14GENIChomozygous54725905
73424351134243512G-26GENIChomozygous54725907
73424361534243616AG48GENIChomozygous54725909
73424368434243685AG42GENIChomozygous54725911
73424373834243739AG32GENIChomozygous54725913
73424405334244054AG34GENIChomozygous54725915
73424411934244120CT40GENIChomozygous54725917
73424442334244424TC47GENICpossibly homozygous54725919
73424447834244479GA37GENICpossibly homozygous54725921
73424488834244889GA30GENIChomozygous54725923
73424609734246098GC24GENIChomozygous54725925
73424681134246812TC28GENIChomozygous54189664
73424686834246869AG28GENIChomozygous54189665
73424687734246878CA31GENIChomozygous54725927