chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145265474145265475GA75GENIChomozygous112870736
4145267429145267430AG49GENIChomozygous112870737
4145268415145268416TC79GENIChomozygous112870738
4145271915145271915A52GENIChomozygous128087945
4145272259145272260GA65GENIChomozygous112870739
4145272261145272262AC68GENIChomozygous112870740
4145273509145273510AG88GENIChomozygous112870741
4145275553145275554CA60GENICpossibly homozygous112870742
4145277091145277092CT71GENIChomozygous112870743
4145277483145277484TC59GENIChomozygous112870744
4145280292145280293CT88GENIChomozygous112870745