chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206436961206436962CCA15GENICheterozygous61066875
1206436962206436963A-15GENICheterozygous61066876
1206437153206437154CT32GENIChomozygous62030963
1206437615206437616CCTG22GENIChomozygous61066877
1206437740206437741CT21GENIChomozygous62030964
1206438198206438199TA24GENIChomozygous61066879
1206439266206439267AAC10GENIChomozygous61066881
1206439311206439312AT14GENIChomozygous62030965
1206440048206440049CT11GENIChomozygous62030966
1206441814206441815TC12GENIChomozygous62030967
1206444396206444397TTA6GENIChomozygous62030968
1206445355206445356CCT4GENIChomozygous62030969
1206446534206446535AT20GENIChomozygous61066884
1206446910206446911TTA11GENIChomozygous62030970
1206447602206447603AATTT10GENICheterozygous61066885
1206447602206447603AATTTT10GENICheterozygous62192828