chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99448686694486867GC2GENIChomozygous52053563
99448752994487530CT14GENIChomozygous52280663
99448836894488369GT24GENIChomozygous52280664
99448868994488707CACACACACACACACACA------------------10GENICheterozygous52915583
99448869194488707CACACACACACACACA----------------10GENICheterozygous52955395
99448966894489669CT16GENIChomozygous52280665
99449027094490271AAG18GENIChomozygous52280666
99449037594490376TC9GENIChomozygous52280667
99449066994490670CA7GENIChomozygous52053575
99449067294490674AA--7GENIChomozygous52280668
99449105094491051AG12GENIChomozygous52053579
99449110194491107ACACAC------4GENIChomozygous52915584
99449138294491383TC6GENIChomozygous52053583
99449201894492019TA22GENIChomozygous52280673
99449204794492048GA22GENIChomozygous52280674
99449228194492282CA23GENIChomozygous52053589
99449246694492467CT28GENIChomozygous52280675
99449249794492498GGCA21GENIChomozygous52053593
99449289394492894G-15GENIChomozygous52280676
99449292194492923TT--19GENICheterozygous52053594
99449293894492939CCT14GENICheterozygous52053598
99449350094493506ACACAC------13GENIChomozygous52280678
99449352294493523AG18GENIChomozygous52280680
99449402494494025GC21GENIChomozygous52280681
99449477494494775CG14GENIChomozygous52280683
99449479694494797AG10GENIChomozygous52053600
99449495694494957CCTG4GENICheterozygous52053602
99449496394494965TG--4GENICheterozygous53145056