chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153176950153176951AG30GENIChomozygous112889324
4153177109153177110CT22GENIChomozygous112889325
4153177340153177341AG20GENIChomozygous119317166
4153177816153177817CT28GENIChomozygous112889327
4153178286153178287CT17GENIChomozygous112889328
4153179792153179793GA16GENIChomozygous112889329
4153180033153180034GA18GENIChomozygous112889330
4153181676153181677AG30GENIChomozygous112889331
4153184832153184833TC25GENIChomozygous112889335
4153185071153185072GA12GENIChomozygous112889336
4153185140153185141AG6GENIChomozygous112889337
4153185545153185546TA17GENIChomozygous112889341
4153186797153186798AC10GENIChomozygous112889342
4153187930153187931CA32GENIChomozygous112889344
4153188052153188053TC27GENIChomozygous112889345
4153188085153188086GA32GENIChomozygous112889346
4153188567153188568TG20GENIChomozygous112889347
4153189416153189417TG18GENIChomozygous112889348
4153189480153189481CT19GENIChomozygous112889349
4153189906153189907CT29GENIChomozygous112889350
4153194434153194435TC28GENIChomozygous112889352
4153194609153194610TC25GENICpossibly homozygous119282179
4153195252153195253GA19GENIChomozygous112889353
4153195847153195848CT7GENIChomozygous112889354