chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22504430825044309AG19GENIChomozygous110490938
22504457825044579CT26GENIChomozygous109649079
22504493125044932GA30GENIChomozygous110490940
22504533525045336AG25GENIChomozygous109649085
22504545025045451TC25GENIChomozygous109649087
22504549825045499AG29GENICpossibly homozygous109649089
22504631225046313CT21GENIChomozygous110490942
22504661825046619AG24GENIChomozygous110490944
22504681025046811CA25GENIChomozygous109649095
22504693425046935TC27GENIChomozygous110490946
22504712725047128CT29GENIChomozygous109649098
22504714625047147AC25GENIChomozygous110490948
22504715425047155TC28GENIChomozygous109649100
22504718425047185CT31GENIChomozygous109649102
22504726825047269CT35GENIChomozygous110490950
22504783525047836CG16GENIChomozygous110490954
22504804825048049CT23GENIChomozygous110490956
22504815225048153CT13GENIChomozygous109649110
22504833825048339GT17GENIChomozygous109649112
22504839725048398AG20GENIChomozygous109649114
22504924525049246AG29GENIChomozygous110490958
22504928225049283AG34GENIChomozygous109649116
22504936425049365AG26GENIChomozygous109649118
22504984325049844CT37GENIChomozygous109649122
22505092925050930AG17GENIChomozygous109649130