chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99448686694486867GC1GENIChomozygous52053563
99448752994487530CT26GENIChomozygous52280663
99448836894488369GT24GENIChomozygous52280664
99448868994488707CACACACACACACACACA------------------10GENICheterozygous52915583
99448966894489669CT28GENIChomozygous52280665
99449027094490271AAG16GENIChomozygous52280666
99449037594490376TC10GENIChomozygous52280667
99449066994490670CA10GENIChomozygous52053575
99449067294490674AA--11GENICheterozygous52280668
99449105094491051AG15GENIChomozygous52053579
99449110194491107ACACAC------10GENICpossibly homozygous52915584
99449138294491383TC12GENIChomozygous52053583
99449201894492019TA17GENIChomozygous52280673
99449204794492048GA15GENIChomozygous52280674
99449228194492282CA16GENIChomozygous52053589
99449246694492467CT27GENIChomozygous52280675
99449249794492498GGCA21GENIChomozygous52053593
99449289394492894G-6GENIChomozygous52280676
99449293894492939CCT6GENICheterozygous52053598
99449350094493506ACACAC------21GENIChomozygous52280678
99449352294493523AG21GENIChomozygous52280680
99449402494494025GC18GENIChomozygous52280681
99449477494494775CG10GENIChomozygous52280683
99449479694494797AG6GENIChomozygous52053600
99449495694494957CCTG5GENIChomozygous52053602