chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124125609341256094TC58GENIChomozygous115384908
124125613441256135AG57GENICpossibly homozygous115384910
124125616241256163GA57GENICpossibly homozygous115384912
124125644741256448GT39GENIChomozygous115384914
124125831141258312AG44GENIChomozygous115384916
124125850041258501TC57GENIChomozygous115384918
124125856741258568AT48GENIChomozygous115384920
124125928741259288CG32GENIChomozygous115384924
124125932141259322TC33GENIChomozygous115384926
124125941141259412CT60GENIChomozygous115384928
124125990841259909TC26GENIChomozygous115441919
124126065341260654AG48GENIChomozygous115384934
124126075341260754GT20GENIChomozygous115384936
124126076941260770GA20GENIChomozygous115384938
124126078041260781AC24GENIChomozygous115384940
124126093541260936TC34GENIChomozygous115441920
124126101741261018CT24GENIChomozygous115384942
124126259841262599CT50GENIChomozygous115384944
124126268141262682GA26GENIChomozygous115384946
124126504641265047CT11GENIChomozygous115384948
124126508141265082CT21GENIChomozygous115384950
124126575041265751CT35GENIChomozygous115384954
124126575141265752CT34GENIChomozygous115384956
124126633741266338GC39GENIChomozygous115384958
124126639441266395CG42GENIChomozygous115384960
124126640941266410CA33GENIChomozygous115384962