chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42710572127105722TTGGAGG8GENIChomozygous56802636
42710599027106002AGACAGACACCT------------1GENIChomozygous56802638
42712279327122794AACTAT17GENICpossibly homozygous56802640
42713670527136706GGT8GENIChomozygous56802642
42714417927144180AAGCTGATGCACTC11GENIChomozygous56802644
42714551527145516AAGT41GENICheterozygous56802646
42716258027162581AG28GENICheterozygous56802648
42716657627166577CCTA10GENIChomozygous56802650
42717862727178628TA24GENICheterozygous56802652
42718215627182158TG--12GENICheterozygous56802654
42720918927209190CCT14GENICheterozygous56802656
42721643827216439GGTGTGTC31GENICpossibly homozygous56802658
42721648727216488GGT38GENIChomozygous56802660
42722742327227424CCTG13GENICheterozygous56802662
42722832927228330C-41GENIChomozygous56802664
42722854927228550TC48GENIChomozygous56802666
42723350527233507AT--8GENICheterozygous56802668