chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103058413830584139AG11GENIChomozygous138754914
103058443130584432AG16GENIChomozygous138754915
103058453230584533GA17GENIChomozygous138754916
103058509030585091CT24GENIChomozygous138754917
103058534330585344CT25GENIChomozygous138754918
103058777530587776TC24GENIChomozygous138754919
103058888030588881CT19GENIChomozygous138754920
103058900330589004AG24GENIChomozygous138754921
103058979230589793AC19GENIChomozygous138754922
103059148330591484AG21GENIChomozygous138754923
103059331130593312TC22GENIChomozygous138754924
103059674530596746CT18GENIChomozygous138754925
103059778030597781TC16GENIChomozygous138754926
103059812130598122CT26GENIChomozygous138754927
103059813030598131GA28GENIChomozygous138754928
103059861330598613GGA19GENIChomozygous138676344
103059883330598834CT14GENIChomozygous138754929
103059906730599068GC23GENIChomozygous138754930
103059909230599093GT24GENIChomozygous138754931
103059917530599176GA24GENIChomozygous138754932
103059930830599309GA14GENIChomozygous138754933
103059947130599472GC13GENIChomozygous138754934
103059976430599765G5GENIChomozygous403280997
103059976430599765GA5GENICheterozygous403280998
103059976030599761G5GENIChomozygous403280995
103059976030599761GC5GENICheterozygous403280996
103059980030599801GC13GENIChomozygous138754935
103059980230599803GT14GENIChomozygous138754936
103060020630600207AG20GENIChomozygous138754937