chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157352689157352690AG36GENIChomozygous112905957
4157352725157352726AG37GENIChomozygous112905959
4157352821157352822TA27GENIChomozygous112905961
4157352848157352849CT29GENIChomozygous112905963
4157353276157353277GA25GENIChomozygous112905965
4157354572157354573GA22GENIChomozygous112905967
4157354730157354731TC22GENIChomozygous112905969
4157355865157355866AC45GENIChomozygous112905971
4157356273157356274TC30GENIChomozygous112905973
4157356310157356311TC32GENIChomozygous112905975
4157356582157356583CA30GENIChomozygous112905977
4157356818157356819GT24GENIChomozygous112905979
4157357313157357314TC23GENIChomozygous112905981
4157357344157357345GA28GENIChomozygous112905983
4157357728157357729AG23GENIChomozygous112905985
4157357992157357993GA32GENIChomozygous112905987
4157358290157358291CT10GENIChomozygous112905989
4157358316157358316G9GENICpossibly homozygous128096094
4157358404157358405GA21GENIChomozygous112905991
4157358594157358595CT30GENIChomozygous112905993
4157358893157358894AC32GENIChomozygous112905995
4157359209157359210CT29GENIChomozygous112905997