chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86448208064482081GT19GENIChomozygous117043682
86448231464482315AG15GENIChomozygous117944623
86448339264483393TC30GENIChomozygous117043683
86448376664483767GA20GENIChomozygous117043685
86448596664485967CT24GENICpossibly homozygous118023213
86448721464487215TC22GENIChomozygous117043689
86448721964487220AG24GENIChomozygous117043690
86448866464488665AG26GENIChomozygous118023215
86448902964489030TC27GENIChomozygous117043692
86448934464489345AG38GENIChomozygous117043693
86448939064489391CT33GENIChomozygous117043694
86449051664490517AC16GENIChomozygous118023217
86449052764490528AT17GENIChomozygous117043695
86449133864491339AG18GENIChomozygous117043696
86449185464491855GC38GENIChomozygous118023219
86449243264492433GA16GENIChomozygous117043697
86449543364495434GT35GENICpossibly homozygous117043700
86449594764495948TC31GENIChomozygous117043702
86449648464496485CA26GENIChomozygous118023221
86449669764496698GC31GENIChomozygous117043704
86449700664497007GT22GENIChomozygous117043705
86449701764497018AG23GENIChomozygous117043706
86449725464497255TC25GENIChomozygous117043707
86449748964497490CT25GENIChomozygous117944629
86450103164501032GA36GENIChomozygous117043709
86450135364501354GA34GENIChomozygous117944630
86450208464502085AG30GENIChomozygous117043710