chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47062521270625213TC11GENIChomozygous113116516
47062650670626507AG52GENIChomozygous113032320
47062667770626678TC39GENIChomozygous113032321
47062685170626852CT36GENIChomozygous113032322
47062690570626906CT45GENIChomozygous113032323
47062707170627072CA58GENIChomozygous113032326
47062707470627075TC56GENICpossibly homozygous113032327
47062736170627362GT34GENIChomozygous113032328
47062742870627429AT23GENIChomozygous113032329
47062753370627534AG41GENIChomozygous113032330
47062774270627743CT36GENIChomozygous113032331
47062779770627798AT37GENIChomozygous113032332
47062784270627843GT30GENIChomozygous113032334
47062789470627895AT36GENIChomozygous113032335
47062790370627904GT38GENIChomozygous113032336
47062795370627954GA39GENIChomozygous113032337
47062808870628089GA44GENIChomozygous113032338
47062810370628104AG39GENICpossibly homozygous113032339
47062812070628121TC42GENICpossibly homozygous113032340
47062819570628196CT41GENIChomozygous113032341
47062823470628235CT44GENIChomozygous113032342
47062828170628282GC49GENIChomozygous113032343
47062831970628320GA41GENIChomozygous113032344
47062844570628446TA43GENIChomozygous113032345