chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2140287335140287336GA14GENIChomozygous110758833
2140288158140288159AT16GENIChomozygous110034638
2140288713140288714GA18GENIChomozygous110758834
2140288769140288770TA16GENIChomozygous110758835
2140289419140289420CT21GENIChomozygous110758836
2140289927140289928GT15GENIChomozygous110034641
2140289953140289954TC10GENIChomozygous110758837
2140289970140289971AG10GENICheterozygous110758838
2140290121140290122GA11GENIChomozygous110758839
2140290143140290144AG15GENIChomozygous110034642
2140290450140290451AC15GENIChomozygous110034648
2140291379140291380CT21GENIChomozygous110758842
2140292941140292942CT17GENICheterozygous110758843
2140292969140292970CT15GENIChomozygous110758844
2140293144140293145GC13GENIChomozygous110758845
2140293174140293175CT12GENIChomozygous110758846
2140293523140293524CT12GENIChomozygous110758847
2140293715140293716CA10GENIChomozygous110034652
2140294096140294097AT17GENIChomozygous110034653
2140294768140294769AC9GENIChomozygous110034654
2140295158140295159TC23GENIChomozygous110758848
2140295532140295533GA10GENIChomozygous110758849
2140296819140296820CG10GENICheterozygous110758850
2140297000140297001AG23GENIChomozygous110034656
2140297008140297009CA21GENIChomozygous110758851
2140297036140297037TG19GENIChomozygous110034657
2140297391140297392CT20GENIChomozygous110758852
2140298706140298707GA5GENIChomozygous110890368
2140299264140299265AC19GENICpossibly homozygous120127200
2140299995140299996CA20GENIChomozygous110758854
2140301156140301157GC18GENIChomozygous110034662
2140302275140302276TC16GENIChomozygous110758855
2140305427140305428CT18GENIChomozygous110034674
2140305442140305443CT17GENIChomozygous110034675
2140306547140306548TC18GENIChomozygous110034677