chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101467837514678376CT44GENIChomozygous116737182
101467869714678698GA23GENIChomozygous116737183
101467905014679051TC36GENIChomozygous116737184
101467907014679071TC37GENIChomozygous116737185
101467926114679262TG24GENIChomozygous116737186
101467930314679304GT23GENIChomozygous116737187
101467935214679353GA27GENIChomozygous116737188
101467956614679567CT38GENIChomozygous116737189
101467992114679922AG41GENIChomozygous116737190
101467994914679950TC40GENIChomozygous116737191
101467997414679975CG38GENIChomozygous116737192
101467999614679997TC35GENIChomozygous116737193
101468000514680006GA39GENIChomozygous116737194
101468001014680011CG41GENIChomozygous116496853
101467920314679204AC25GENIChomozygous116496849
101467975514679756AC33GENIChomozygous116496851
101467938114679420CCCATAAAACACCTGGGATACCTGGTACTTCTGAGACAC32GENIChomozygous131088063
101467978114679782TC39GENIChomozygous116859733
101467980314679804CT32GENIChomozygous116859735
101467982614679827CT32GENIChomozygous116859737
101468003814680039AG48GENICpossibly homozygous116737195
101468005114680052GC44GENICpossibly homozygous116737196
101468015214680153AC52GENICpossibly homozygous116859739
101468027114680272TG31GENIChomozygous116737197
101468032814680328G33GENICpossibly homozygous131088064
101468033614680336CAGAAAGCCTGGAC32GENICpossibly homozygous131088065
101468034114680341AAGGTTGTTCTAG32GENICpossibly homozygous131088066
101468048714680488TC42GENIChomozygous116737198
101468054914680550C41GENIChomozygous131088067
101468129414681295CT34GENIChomozygous116737199
101468131414681314CTC36GENIChomozygous131088068
101468139514681396TC33GENIChomozygous116496855
101468156214681563TC44GENIChomozygous116496857
101468186514681866TC24GENIChomozygous116496859