chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206436961206436962CCA8GENICpossibly homozygous61066875
1206437153206437154CT20GENIChomozygous62030963
1206437615206437616CCTG34GENIChomozygous61066877
1206437740206437741CT28GENIChomozygous62030964
1206438198206438199TA17GENIChomozygous61066879
1206439311206439312AT17GENIChomozygous62030965
1206440048206440049CT17GENIChomozygous62030966
1206441814206441815TC27GENIChomozygous62030967
1206444396206444397TTA16GENIChomozygous62030968
1206445355206445356CCT10GENIChomozygous62030969
1206446534206446535AT24GENIChomozygous61066884
1206439266206439267AAC8GENIChomozygous61066881
1206446910206446911TTA7GENICpossibly homozygous62030970
1206447602206447603AATTT2GENICheterozygous61066885
1206447602206447603AATTTT2GENICheterozygous62192828
1206449232206449233GGGC24GENICheterozygous62236457
1206449236206449238CC--23GENICheterozygous62236458