chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140623027140623028CT16GENIChomozygous113057182
4140628158140628159TC17GENIChomozygous112857824
4140631274140631275CT15GENIChomozygous113057194
4140631902140631903TC23GENIChomozygous112857844
4140635877140635878AG13GENIChomozygous112857854
4140636187140636188GA23GENIChomozygous113057196
4140637050140637051TA16GENIChomozygous112857856
4140637102140637103GA11GENIChomozygous119359105
4140637456140637457AT6GENIChomozygous112857858
4140637859140637860TC29GENIChomozygous112857860
4140638287140638288AG28GENIChomozygous112857862
4140639620140639621TG27GENIChomozygous112857866
4140640261140640262CA29GENIChomozygous113057200
4140641779140641780TC19GENIChomozygous112857876
4140642196140642197GA19GENIChomozygous113057208
4140642217140642218CT16GENIChomozygous113057210
4140642631140642632CG9GENIChomozygous112857878
4140643047140643048GA22GENIChomozygous112857880
4140645514140645515CA14GENIChomozygous112857882
4140645776140645777GA28GENIChomozygous112857884
4140648886140648887GA15GENIChomozygous112857888
4140649329140649330CG11GENIChomozygous112857890
4140649516140649517AT20GENIChomozygous112857892
4140651537140651538CG40GENIChomozygous112857894
4140652389140652390TC37GENIChomozygous112857898
4140652661140652662TG21GENIChomozygous113057218
4140654061140654062AT27GENIChomozygous112857902
4140654756140654757GA21GENIChomozygous112857904