chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47062521270625213TC4GENIChomozygous113116516
47062601670626017TC16GENIChomozygous113349581
47062650670626507AG27GENIChomozygous113032320
47062667770626678TC23GENIChomozygous113032321
47062685170626852CT31GENIChomozygous113032322
47062707170627072CA38GENIChomozygous113032326
47062707470627075TC39GENIChomozygous113032327
47062736170627362GT41GENIChomozygous113032328
47062742870627429AT24GENIChomozygous113032329
47062753370627534AG16GENIChomozygous113032330
47062771770627718GT24GENIChomozygous113349583
47062774270627743CT26GENIChomozygous113032331
47062777470627775TG19GENICpossibly homozygous113349585
47062784270627843GT20GENIChomozygous113032334
47062789470627895AT16GENIChomozygous113032335
47062790370627904GT16GENIChomozygous113032336
47062795370627954GA13GENIChomozygous113032337
47062808870628089GA17GENIChomozygous113032338
47062810370628104AG18GENIChomozygous113032339
47062812070628121TC14GENIChomozygous113032340
47062819570628196CT15GENIChomozygous113032341
47062823470628235CT15GENIChomozygous113032342
47062828170628282GC16GENIChomozygous113032343
47062831970628320GA19GENIChomozygous113032344
47062844570628446TA36GENIChomozygous113032345