chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115255608115255609AC14GENIChomozygous112815031
4115258594115258595TC18GENIChomozygous112815035
4115258679115258680GC22GENIChomozygous112815037
4115258687115258688GA25GENIChomozygous112815039
4115261930115261931AG34GENIChomozygous112815043
4115262141115262142GA31GENIChomozygous112815045
4115265585115265586AG23GENIChomozygous112815047
4115269353115269354CT26GENIChomozygous112815049
4115270254115270255GA22GENIChomozygous112815051
4115270764115270765AC18GENIChomozygous112815053
4115271633115271634AC18GENIChomozygous112815055
4115272999115273000AC27GENIChomozygous112815059
4115274349115274350CG27GENIChomozygous112815061
4115274808115274809TC23GENIChomozygous112815063
4115275324115275325GT22GENIChomozygous112815065
4115275502115275503GT37GENIChomozygous112815067
4115275511115275512GA35GENIChomozygous112815069
4115275873115275874GA38GENIChomozygous112815071
4115276334115276335TC31GENIChomozygous112815073
4115276963115276964CT28GENIChomozygous112815075
4115276986115276987GA30GENIChomozygous119454567