chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144441641344416413T29GENIChomozygous129152856
144441786744417868TC34GENIChomozygous113444658
144441787644417877GA34GENIChomozygous113444660
144441851244418513TA32GENIChomozygous113444662
144442348644423487G27GENIChomozygous129152857
144442457644424580TTCA31GENIChomozygous130140160
144442769144427691A26GENICpossibly homozygous129152858
144443078644430788TA4GENIChomozygous129152859
144443323444433236AC18GENICheterozygous130140161
144443610644436107CT5GENICheterozygous118691616
144444369544443696TC37GENIChomozygous113444664
144444369644443697AT37GENIChomozygous113444666
144444394544443946TC33GENIChomozygous113444668
144444606044446060T35GENICheterozygous129152860
144445198344451984GT9GENIChomozygous118794974
144445771744457718AG39GENIChomozygous113444670
144443080644430807CT1GENIChomozygous114155145