chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121811393718113938AAC19GENIChomozygous691212350
121811672718116728AG34GENICpossibly homozygous521737087
121811745318117454TC23GENIChomozygous523320765
121811749118117492GGT21GENICpossibly homozygous691212351
121811749418117495G-20GENICpossibly homozygous691212352
121811792618117927TA41GENIChomozygous521737088
121811839518118396AAC30GENIChomozygous691212353
121811888318118884GA35GENIChomozygous521737089
121811929718119299GG--24GENIChomozygous691212354
121811989218119893AAT21GENIChomozygous691212355
121811990518119906TC22GENIChomozygous521737090
121812018018120181CCA41GENIChomozygous691212356
121812220618122207CA33GENIChomozygous521737091
121812240618122407GA50GENICpossibly homozygous521737092
121812290118122902AG18GENIChomozygous521737093