chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124125604241256043TC19GENIChomozygous115384906
124125609341256094TC24GENIChomozygous115384908
124125613441256135AG26GENIChomozygous115384910
124125616241256163GA21GENIChomozygous115384912
124125644741256448GT18GENIChomozygous115384914
124125831141258312AG26GENICpossibly homozygous115384916
124125850041258501TC23GENIChomozygous115384918
124125856741258568AT21GENIChomozygous115384920
124125903041259031TC23GENIChomozygous115477941
124125928741259288CG26GENIChomozygous115384924
124125932141259322TC20GENIChomozygous115384926
124125941141259412CT19GENIChomozygous115384928
124125965141259652GC24GENIChomozygous115384930
124125965541259656AT26GENIChomozygous115384932
124126065341260654AG26GENIChomozygous115384934
124126075341260754GT19GENIChomozygous115384936
124126076941260770GA16GENIChomozygous115384938
124126078041260781AC18GENIChomozygous115384940
124126101741261018CT27GENIChomozygous115384942
124126004441260045AG11GENIChomozygous115329742
124125990841259909TC13GENIChomozygous115441919
124126093541260936TC28GENIChomozygous115441920
124126259841262599CT18GENIChomozygous115384944
124126268141262682GA27GENIChomozygous115384946
124126410241264103CT25GENIChomozygous115329750
124126504641265047CT20GENIChomozygous115384948
124126508141265082CT20GENIChomozygous115384950
124126563941265640CT21GENIChomozygous115384952
124126575041265751CT24GENIChomozygous115384954
124126575141265752CT23GENIChomozygous115384956
124126633741266338GC16GENIChomozygous115384958
124126639441266395CG15GENIChomozygous115384960
124126640941266410CA14GENIChomozygous115384962