chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140623027140623028CT13GENIChomozygous113057182
4140624176140624177GA9GENIChomozygous113057184
4140628158140628159TC8GENIChomozygous112857824
4140631274140631275CT15GENIChomozygous113057194
4140631902140631903TC25GENIChomozygous112857844
4140635877140635878AG9GENIChomozygous112857854
4140636187140636188GA13GENIChomozygous113057196
4140637153140637154AT3GENIChomozygous119442131
4140637154140637155GT3GENIChomozygous119442132
4140637859140637860TC23GENIChomozygous112857860
4140638287140638288AG18GENIChomozygous112857862
4140639620140639621TG20GENIChomozygous112857866
4140640261140640262CA16GENIChomozygous113057200
4140641779140641780TC23GENIChomozygous112857876
4140642196140642197GA13GENIChomozygous113057208
4140642217140642218CT15GENIChomozygous113057210
4140642631140642632CG21GENIChomozygous112857878
4140643047140643048GA22GENIChomozygous112857880
4140645514140645515CA22GENIChomozygous112857882
4140645776140645777GA24GENIChomozygous112857884
4140648886140648887GA13GENIChomozygous112857888
4140649329140649330CG12GENIChomozygous112857890
4140649516140649517AT18GENIChomozygous112857892
4140651537140651538CG20GENIChomozygous112857894
4140652389140652390TC17GENICpossibly homozygous112857898
4140652661140652662TG24GENIChomozygous113057218
4140654061140654062AT27GENIChomozygous112857902
4140654756140654757GA24GENIChomozygous112857904