chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104705740447057405TG11GENIChomozygous51445583
104705778447057785CT11GENIChomozygous51445585
104705816347058176GCTGGGCCTTGTG-------------8GENIChomozygous51445586
104705865347058657GCCC----12GENIChomozygous52053895
104706012147060122AG10GENIChomozygous52053897
104706220947062210AC9GENIChomozygous52053899
104706281847062819CT13GENIChomozygous52053901
104706309647063097AG11GENIChomozygous51637340
104706370047063701AG12GENIChomozygous51445588
104706411747064118GA14GENIChomozygous51637341
104706411947064120CT14GENIChomozygous51637342
104706549647065497CT17GENIChomozygous52053903
104706552747065528TA19GENIChomozygous52053905
104706622847066229CT14GENIChomozygous52053907
104706736747067368GA17GENIChomozygous52053909
104706789547068005CATCCATCCATCCATCCATCCATCATCCACCCATGTATCCATCCATCCATCCATCCATCCATCCATCCATCCACTCATGTATCCATCCATCCATCCATCCATCCATCCAT--------------------------------------------------------------------------------------------------------------13GENICheterozygous53526374
104707130447071305CT14GENIChomozygous52053911
104707156847071569GT17GENIChomozygous52053913
104707227647072278CT--10GENIChomozygous52053915
104707870947078710TC7GENIChomozygous51637378
104708242847082429GT14GENIChomozygous52053927
104708257947082580AT7GENIChomozygous51445604
104708326147083262C-15GENIChomozygous51637388
104708360347083604CCT11GENIChomozygous52053929
104708400747084008TC7GENIChomozygous52053931
104708414647084147AAT11GENIChomozygous52053933
104708471247084713TC12GENIChomozygous52053935
104708496047084961GA13GENIChomozygous52053937
104708766247087663AT14GENIChomozygous52053941
104708805947088060GA14GENIChomozygous52053943
104708898347088984TA15GENIChomozygous52053945
104708900347089004GT18GENIChomozygous52053947
104709157747091578GC7GENIChomozygous51637395
104709235347092354CT16GENIChomozygous52053951
104709256447092565GA18GENIChomozygous51637397
104711236747112368GA10GENIChomozygous52053953
104711434847114353AAAAC-----10GENIChomozygous51876135