chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175079202550792026CT17GENIChomozygous580069044
175079206850792069GC23GENIChomozygous580069045
175079220550792206CG20GENIChomozygous580069046
175079260250792603GA23GENIChomozygous580069047
175079281050792811AG24GENIChomozygous580069048
175079289550792896AG16GENIChomozygous580069049
175079310250793103TTA3GENICheterozygous717247287
175079315150793152AC5GENIChomozygous580069050
175079318450793185AG7GENIChomozygous580069051
175079326350793264T-7GENICheterozygous717247288
175079331450793315TC10GENICpossibly homozygous580069052
175079332850793329CT11GENIChomozygous580069053
175079337850793379CT12GENIChomozygous580069054
175079341450793415AG24GENIChomozygous580069055
175079369550793696CT16GENICheterozygous580069056
175079369650793697GA16GENICheterozygous580069057
175079393650793937AC11GENICheterozygous580069058
175079452150794522GC2GENIChomozygous580069059
175079452850794529GA2GENIChomozygous580069060
175079453750794538CT2GENIChomozygous580069061
175079505850795059GA11GENIChomozygous580069062
175079520050795201TC16GENIChomozygous580069063
175079567650795677CT28GENICpossibly homozygous580069064
175079672750796728GA14GENIChomozygous580069065
175079678550796786CT7GENICheterozygous580069066
175079713550797136TC15GENIChomozygous580304536
175079759550797596CT28GENICpossibly homozygous580069067
175079842150798422TTGC4GENICheterozygous717247289
175079852150798522CT13GENIChomozygous580069068
175080012550800126AG22GENIChomozygous580069069