chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1109727493109727494TC14GENIChomozygous60789712
1109727818109727819TC4GENICheterozygous60789713
1109728936109728937A-16GENICpossibly homozygous60789714
1109729045109729046TG22GENIChomozygous60789715
1109729455109729456TC13GENICpossibly homozygous60789716
1109730351109730352CCT7GENIChomozygous60789718
1109730361109730362CA3GENIChomozygous60789719
1109730562109730563AG24GENICpossibly homozygous60789722
1109730587109730588CT19GENIChomozygous62570897
1109730648109730649GGA5GENICheterozygous60789723
1109727954109727955AAT7GENIChomozygous61500180
1109729642109729643TC21GENIChomozygous61500181
1109730421109730422TC12GENIChomozygous61500182
1109729826109729827GA17GENICpossibly homozygous62690757
1109731470109731471AT9GENIChomozygous60789725
1109731617109731618TC26GENICheterozygous60789726
1109731920109731921TA18GENIChomozygous60789727
1109732178109732179AG18GENIChomozygous60789728
1109732279109732280CG19GENICpossibly homozygous60789729
1109733501109733502TTA22GENICheterozygous62085829
1109733504109733505TTA24GENICheterozygous62085830
1109733509109733510CCA25GENICheterozygous62085831
1109733531109733532TC18GENICpossibly homozygous60789731
1109733563109733567GTTT----5GENIChomozygous60789732