chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206436961206436962CCA12GENICheterozygous61066875
1206436962206436963A-12GENICheterozygous61066876
1206437615206437616CCTG28GENIChomozygous61066877
1206437859206437860AG24GENIChomozygous61066878
1206438198206438199TA31GENIChomozygous61066879
1206438842206438843AATACT24GENIChomozygous61066880
1206439266206439267AAC9GENIChomozygous61066881
1206441025206441027TG--22GENIChomozygous61066882
1206446279206446280TTTTTTA4GENIChomozygous61066883
1206446534206446535AT28GENIChomozygous61066884
1206447539206447540T-1GENIChomozygous61802925
1206447602206447603AATTT7GENICheterozygous61066885
1206447602206447603AATT7GENICheterozygous61066886
1206447774206447775A-2GENIChomozygous61066887
1206449281206449282TC32GENICheterozygous61921335
1206449233206449234AG38GENICheterozygous61921333
1206449253206449254GA35GENICheterozygous61921334