chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141041132141041133CT55GENIChomozygous115939685
7141041404141041405A27GENICpossibly homozygous128529393
7141041587141041588AT44GENIChomozygous115939686
7141045765141045765A45GENICpossibly homozygous128529395
7141046228141046229CT60GENIChomozygous116232949
7141052572141052573C20GENIChomozygous128529396
7141053521141053522CG48GENIChomozygous115939690
7141054282141054283AG82GENIChomozygous115939691
7141045805141045806CT61GENIChomozygous132991391
7141046935141046941GTGTGC19GENIChomozygous132985726
7141053023141053030CGGAGGG55GENIChomozygous132985727
7141056967141056968GA61GENIChomozygous118288094
7141055733141055734CT60GENIChomozygous118288092
7141042089141042090AT49GENIChomozygous118288086
7141051116141051117AC63GENIChomozygous118288088
7141051758141051759GA56GENICpossibly homozygous118288090
7141059490141059491GA76GENIChomozygous118288096
7141059825141059826AG70GENICpossibly homozygous118288098
7141060510141060511AG59GENIChomozygous115939693
7141061014141061015TA63GENIChomozygous118288100
7141061219141061219C39GENICpossibly homozygous128529397
7141062476141062480TTCA37GENICpossibly homozygous132985728
7141062509141062510GT46GENIChomozygous118288102
7141063700141063700TGTT47GENIChomozygous128529399
7141065201141065202CT53GENIChomozygous118288106
7141065297141065298AC48GENIChomozygous118288108
7141065334141065335CA48GENIChomozygous118288110
7141066029141066030TC66GENIChomozygous115939695
7141066780141066781CT58GENIChomozygous115939696
7141067470141067471TC63GENIChomozygous118288112
7141068701141068702CT54GENIChomozygous118288114
7141069363141069363TTTTTTAAATTGTCAACCGTTGTTACTGATTGGTCTCC48GENIChomozygous128529401
7141069626141069627CT50GENIChomozygous118288116
7141069637141069637G47GENIChomozygous128529402
7141062434141062442GTTTGTTT33GENIChomozygous132658984