chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206436961206436962CCA18GENICheterozygous61066875
1206436962206436963A-18GENICheterozygous61066876
1206437615206437616CCTG48GENIChomozygous61066877
1206437859206437860AG65GENIChomozygous61066878
1206438198206438199TA57GENIChomozygous61066879
1206438842206438843AATACT50GENIChomozygous61066880
1206439266206439267AAC7GENIChomozygous61066881
1206441025206441027TG--50GENIChomozygous61066882
1206446279206446280TTTTTTA8GENICpossibly homozygous61066883
1206446534206446535AT60GENIChomozygous61066884
1206447602206447603AATTT18GENICheterozygous61066885
1206447602206447603AATT18GENICheterozygous61066886
1206447774206447775A-4GENIChomozygous61066887