chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102928078102928079TTGAGCCATG10GENIChomozygous51587870
10102928092102928093T-7GENIChomozygous51587872
10102928170102928171GT9GENIChomozygous51587874
10102928172102928173GT9GENIChomozygous51587876
10102928182102928183GT10GENIChomozygous51587878
10102928185102928186GT10GENIChomozygous51587880
10102928187102928188AT10GENIChomozygous51587882
10102928192102928193GT10GENIChomozygous51587884
10102928196102928197CT10GENIChomozygous51587886
10102928213102928214AT9GENIChomozygous51587888
10102928216102928221CGCCT-----6GENIChomozygous51587890
10102928525102928526T-26GENICheterozygous51942131
10102930724102930725TTGAG3GENIChomozygous51587892
10102930726102930728TC--3GENIChomozygous51587894
10102941651102941652T-19GENICheterozygous51942265
10102948574102948575GA29GENIChomozygous51587900
10102938970102938971C-1GENIChomozygous51587896
10102948478102948479CCTA26GENIChomozygous51587898
10102948588102948589TG29GENIChomozygous51587902
10102949235102949236CT35GENIChomozygous51587904
10102949236102949237CT36GENIChomozygous51587906
10102949905102949906GGCA19GENIChomozygous51587908
10102949945102949946TA16GENIChomozygous51587910
10102949965102949966TC19GENIChomozygous51587912
10102949976102949977GC21GENIChomozygous51587914
10102949990102949991TC27GENIChomozygous51587916
10102950109102950110TC28GENICpossibly homozygous51587918
10102950113102950114TC30GENICpossibly homozygous51587920
10102950131102950132GC32GENIChomozygous51587922
10102950152102950153GC30GENIChomozygous51587924
10102950160102950161TC28GENIChomozygous51587926
10102950318102950319GC18GENIChomozygous51587928
10102950321102950322TC18GENIChomozygous51587930
10102950624102950625CT55GENICpossibly homozygous51587934
10102950650102950651G-53GENIChomozygous51587936
10102953377102953378AAG33GENIChomozygous51587940