chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226047490226047501CACCGTCTTCT-----------1GENIChomozygous61103587
1226047953226047954TC15GENICpossibly homozygous61103588
1226048725226048726CT14GENICpossibly homozygous61103589
1226048905226048906GA27GENICpossibly homozygous61103590
1226049995226049996TC3GENIChomozygous61103591
1226050005226050006TC1GENIChomozygous61103592
1226050637226050638CCTT2GENICheterozygous61103596
1226050648226050649CCTT2GENICheterozygous61103597
1226050986226050987AG25GENICpossibly homozygous61103598
1226051229226051230GA7GENIChomozygous61103599
1226051403226051404TC20GENIChomozygous61103600
1226051557226051558GA6GENICheterozygous61103601
1226052726226052727AAT5GENICheterozygous61103602
1226053774226053775CT25GENIChomozygous61103603
1226054132226054133AG19GENICpossibly homozygous61103604