chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145265474145265475GA58GENIChomozygous112870736
4145267429145267430AG56GENIChomozygous112870737
4145268415145268416TC60GENICpossibly homozygous112870738
4145272259145272260GA62GENIChomozygous112870739
4145272261145272262AC62GENIChomozygous112870740
4145273509145273510AG73GENIChomozygous112870741
4145275553145275554CA65GENICpossibly homozygous112870742
4145277091145277092CT52GENIChomozygous112870743
4145277483145277484TC58GENIChomozygous112870744
4145280292145280293CT80GENIChomozygous112870745
4145271915145271915A83GENIChomozygous128087945