chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410379824103799AC15GENIChomozygous887578126
142410385724103858AT12GENIChomozygous887578125
142410426924104270AG16GENIChomozygous887578124
142410436524104366AG12GENIChomozygous887578123
142410441424104415CG16GENIChomozygous887578122
142410456224104563CT9GENIChomozygous887578121
142410471624104717CT17GENIChomozygous887578120
142410474024104741AG6GENIChomozygous887578119
142410961224109613AG8GENIChomozygous887578118
142410964024109641GA13GENIChomozygous887578117
142410982124109822CA13GENIChomozygous887578116
142410989224109893CA19GENIChomozygous887578115
142410998824109989CG12GENIChomozygous887578114
142411021224110213CT8GENICheterozygous887578113
142411608824116089GC13GENIChomozygous887578112
142411653524116536AG5GENIChomozygous887578111
142411704324117044TG9GENIChomozygous887578110
142411943624119437AT8GENIChomozygous887578109
142411988624119887CT14GENIChomozygous887578108
142412123524121236CT8GENIChomozygous887578107
142412148524121486CT17GENIChomozygous887578106
142412186724121868TA20GENIChomozygous887578105
142412329024123291CA20GENIChomozygous887578104
142412331124123312CG10GENIChomozygous887578103
142412388924123890CG22GENIChomozygous887578102
142412462624124627TC6GENIChomozygous887578101
142412524024125241AG13GENIChomozygous887578100