chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86393424263934243GGT18GENICheterozygous684228589
86393445663934458CC--15GENICheterozygous684228590
86393729663937297AT45GENIChomozygous506088622
86394086663940867GGC16GENICheterozygous684228591
86395503363955034GGAA1GENIChomozygous684228593
86396067963960680GGA1GENIChomozygous684228594
86396485963964860GGT11GENICheterozygous684228596
86397174363971744GGA12GENICheterozygous684228597
86397546163975462AG28GENIChomozygous506088623
86398664163986642GGAA2GENIChomozygous684228598
86399695163996952GGA19GENICheterozygous684228601
86399833963998343CGCG----14GENICheterozygous684228602
86399834163998343CG--14GENICpossibly homozygous684228603
86400084964000852CTA---7GENIChomozygous684228604
86400086364000864CT8GENIChomozygous506088624
86400086664000867CT7GENIChomozygous506088625
86400087964000880GA5GENIChomozygous506088626
86400089464000895C-3GENIChomozygous684228605
86400089664000897CCA3GENIChomozygous684228606
86400897464008975AAGT3GENICheterozygous684228607
86401100664011007CCTT1GENIChomozygous684228608
86401216864012169GT26GENICheterozygous506088627
86401217064012171CT24GENICheterozygous506088628
86402045864020460CA--5GENICheterozygous684228610
86402321364023214CCTTT10GENICheterozygous684228611
86402321364023214CCTT10GENICheterozygous684228613