chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84357134243571343GGA36GENIChomozygous53104299
84357253143572532TG41GENIChomozygous52607677
84357265743572658C-23GENICheterozygous53181414
84357290443572905CCGT2GENIChomozygous53269697
84357353543573536CA32GENIChomozygous52607687
84357353643573537GA32GENICpossibly homozygous52607689
84357354243573543TTG21GENIChomozygous52607691
84357354443573545GA23GENICpossibly homozygous52607693
84357354843573549C-17GENIChomozygous52607694
84357355843573559G-20GENIChomozygous52607696
84357358143573582AC24GENIChomozygous52607698
84357358343573584CT25GENIChomozygous52607700
84357359543573596AC22GENIChomozygous52966248
84357359843573599CCA17GENIChomozygous52607702
84357361043573611GA16GENICpossibly homozygous52607704
84357361243573613GA16GENIChomozygous52607706
84357361843573619GC18GENICpossibly homozygous52607708
84357362743573628GA20GENIChomozygous52607710
84357362943573630AC20GENIChomozygous52607712
84357648443576485CT43GENIChomozygous53316745
84357747743577478AG55GENIChomozygous52607727
84357872043578721TC48GENICpossibly homozygous52607737
84358561443585615TTG26GENICheterozygous53203559
84359022043590221AG53GENICheterozygous53316746
84359709543597096CCGTGT8GENIChomozygous53203572
84360651043606511GGTAA38GENICheterozygous53104388
84360933943609341AA--1GENIChomozygous53104395
84361239943612400AAAAAAATTATTT18GENICheterozygous52607900
84362429443624295AAGT3GENICheterozygous53316747
84362627843626279AG37GENICheterozygous52607930