chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT3GENIChomozygous768388424
162486313224863133TA10GENIChomozygous669260433
162486320324863204TA12GENICpossibly homozygous669260434
162486376124863762GA16GENIChomozygous669260435
162486389124863892GC4GENIChomozygous669260436
162486399024863991GGT3GENICheterozygous768388425
162486527524865276A-19GENIChomozygous768388426
162486561624865617CT8GENIChomozygous669260437
162486670024866701TC9GENICheterozygous669260438
162486680224866803CT18GENICpossibly homozygous669260439
162486702724867028CCT16GENIChomozygous768388427
162486775724867758AG26GENIChomozygous669260440
162486855024868551CT17GENIChomozygous669260441
162486918724869188CT12GENIChomozygous669260442
162486920124869202GA11GENIChomozygous669260443
162486940724869408TA10GENICheterozygous669260444
162486964924869653TAAG----5GENIChomozygous768388428
162486971724869718GC15GENIChomozygous669260445
162486974824869749A-12GENIChomozygous768388429
162487027424870275CG16GENIChomozygous669260446
162487169924871700CT4GENIChomozygous669260447
162487173724871738CA2GENIChomozygous669260448