chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165389475165389476CT25GENIChomozygous108954365
1165396856165396857CT15GENIChomozygous108954366
1165412218165412219CT23GENIChomozygous108954367
1165429727165429728GA21GENIChomozygous108954368
1165430551165430552GA30GENICpossibly homozygous108751491
1165431553165431554GT13GENIChomozygous108954369
1165432058165432059GA23GENIChomozygous108954370
1165433222165433223GC21GENIChomozygous108353603
1165437208165437209AG17GENIChomozygous108353611
1165440669165440670GA29GENIChomozygous108954371
1165434571165434572GA10GENICheterozygous109051895
1165462060165462061AC18GENIChomozygous108353839
1165463085165463086AG21GENIChomozygous108353847
1165464534165464535AT22GENIChomozygous108954372
1165466142165466143AG22GENIChomozygous108353855
1165467121165467122AG28GENIChomozygous108353857
1165470092165470093AG29GENIChomozygous108954373
1165470303165470304CT23GENIChomozygous108353863
1165470739165470740GC41GENICheterozygous108353869
1165471544165471545GA40GENIChomozygous108353871
1165471830165471831TA15GENIChomozygous108954374
1165472448165472449GA25GENIChomozygous108954375
1165472843165472844CT12GENIChomozygous108353877
1165472901165472902TC20GENIChomozygous108353879
1165473190165473191CA26GENICheterozygous108751493
1165473653165473654GA37GENIChomozygous108353881
1165474176165474177AG32GENIChomozygous108353883
1165475318165475319GA29GENIChomozygous108353887
1165476027165476028GA32GENIChomozygous108353889
1165476588165476589GA31GENIChomozygous108353891
1165477011165477012GA36GENIChomozygous108353893
1165477812165477813AC29GENICpossibly homozygous108353897
1165477919165477920AG35GENICpossibly homozygous108353899
1165477997165477998GA25GENIChomozygous108353901
1165479680165479681GA42GENIChomozygous108353907
1165479837165479838GA13GENIChomozygous108353909
1165480010165480011CT23GENIChomozygous108353911