chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193695639036956391TTA18GENICpossibly homozygous46109861
193695692136956922AAGAC21GENICheterozygous46109862
193695715636957157GGT13GENICpossibly homozygous46109863
193695748136957482A-14GENIChomozygous46109864
193695906836959069GA29GENIChomozygous46109865
193695983236959834AA--18GENICpossibly homozygous46109866
193695988036959881CCAG10GENICpossibly homozygous46109867
193696117836961179CCA10GENICheterozygous46249551
193696132936961330TG26GENIChomozygous46109868
193696386036963861CT30GENIChomozygous46109869
193696761136967612CG30GENIChomozygous46109870
193696918736969191GTTC----19GENICheterozygous46109871
193696919036969191C-19GENICheterozygous46109872
193697030336970304GA23GENIChomozygous46109873
193697059736970598AAT29GENIChomozygous46109874
193697120436971205TA38GENIChomozygous46109875
193697170736971708CT28GENIChomozygous46109876
193697231336972314GA28GENIChomozygous46109877
193697295536972956CT20GENIChomozygous46109878
193697500836975012TATT----10GENIChomozygous46109881
193697622036976221AG39GENIChomozygous46109882