chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99448686694486867GC4GENIChomozygous52053563
99448752994487530CT23GENIChomozygous52280663
99448836894488369GT24GENIChomozygous52280664
99448868994488707CACACACACACACACACA------------------10GENICheterozygous52915583
99448966894489669CT23GENIChomozygous52280665
99449027094490271AAG12GENIChomozygous52280666
99449037594490376TC13GENIChomozygous52280667
99449066994490670CA11GENIChomozygous52053575
99449067294490674AA--11GENICpossibly homozygous52280668
99449105094491051AG21GENIChomozygous52053579
99449110194491107ACACAC------10GENICheterozygous52915584
99449110394491107ACAC----10GENICheterozygous53048171
99449138294491383TC20GENIChomozygous52053583
99449201894492019TA25GENIChomozygous52280673
99449204794492048GA31GENIChomozygous52280674
99449228194492282CA27GENIChomozygous52053589
99449246694492467CT33GENIChomozygous52280675
99449249794492498GGCA24GENIChomozygous52053593
99449289394492894G-13GENIChomozygous52280676
99449350094493506ACACAC------20GENIChomozygous52280678
99449352294493523AG30GENIChomozygous52280680
99449402494494025GC22GENIChomozygous52280681
99449477494494775CG14GENIChomozygous52280683
99449479694494797AG10GENIChomozygous52053600
99449495694494957CCTG3GENIChomozygous52053602