chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206436961206436962CCA5GENICheterozygous61066875
1206437153206437154CT24GENIChomozygous62030963
1206437615206437616CCTG28GENIChomozygous61066877
1206437740206437741CT32GENIChomozygous62030964
1206438198206438199TA19GENIChomozygous61066879
1206439266206439267AAC3GENIChomozygous61066881
1206439311206439312AT9GENIChomozygous62030965
1206440048206440049CT18GENIChomozygous62030966
1206441814206441815TC24GENIChomozygous62030967
1206444396206444397TTA10GENIChomozygous62030968
1206445355206445356CCT6GENIChomozygous62030969
1206446534206446535AT29GENIChomozygous61066884
1206446910206446911TTA20GENIChomozygous62030970
1206447602206447603AATTT2GENIChomozygous61066885
1206449281206449282TC32GENICheterozygous61921335
1206449233206449234AG35GENICheterozygous61921333
1206449253206449254GA35GENICheterozygous61921334