chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157352689157352690AG26GENIChomozygous112905957
4157352725157352726AG26GENIChomozygous112905959
4157352821157352822TA20GENIChomozygous112905961
4157352848157352849CT18GENIChomozygous112905963
4157353276157353277GA13GENIChomozygous112905965
4157354572157354573GA19GENIChomozygous112905967
4157354730157354731TC21GENIChomozygous112905969
4157355865157355866AC18GENIChomozygous112905971
4157356273157356274TC18GENIChomozygous112905973
4157356310157356311TC22GENIChomozygous112905975
4157356582157356583CA21GENIChomozygous112905977
4157356818157356819GT22GENIChomozygous112905979
4157357313157357314TC21GENIChomozygous112905981
4157357344157357345GA21GENIChomozygous112905983
4157357728157357729AG17GENIChomozygous112905985
4157357992157357993GA26GENIChomozygous112905987
4157358290157358291CT7GENIChomozygous112905989
4157358404157358405GA15GENIChomozygous112905991
4157358594157358595CT23GENIChomozygous112905993
4157358893157358894AC26GENIChomozygous112905995
4157359209157359210CT20GENIChomozygous112905997
4157358316157358316G7GENIChomozygous128096094