chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1268999661268999662CA4GENIChomozygous61684453
1269009094269009095C-4GENICheterozygous61209668
1269013735269013736GGTC3GENICheterozygous61818351
1269026179269026180C-5GENICheterozygous62251379
1269046340269046342GG--1GENIChomozygous61684455
1269065408269065409TG4GENICheterozygous61643685
1269089693269089694CT12GENIChomozygous61818354
1269089811269089812AG17GENICpossibly homozygous61210032
1269090804269090805CT12GENIChomozygous61818355
1269096790269096791AAT3GENIChomozygous61210082
1269102121269102122CG3GENIChomozygous61818356
1269105333269105334TC2GENIChomozygous61210100
1269121519269121520CT8GENICheterozygous61210173