chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91722796217227962C43GENIChomozygous128685083
91722805317228053T51GENIChomozygous128685084
91722806117228064CCT51GENIChomozygous128685085
91722909417229095G39GENIChomozygous128685086
91722910817229108G38GENIChomozygous128685087
91722911617229117TG39GENIChomozygous117682184
91722911717229118GT38GENIChomozygous117682186
91722912617229127T36GENIChomozygous128685088
91722913117229131T36GENIChomozygous128685089
91722919417229194G42GENIChomozygous128685090
91722919617229197T42GENIChomozygous128685091
91722920417229206TC44GENIChomozygous128685092
91722922917229230T39GENIChomozygous128685093
91722925317229254A37GENIChomozygous128685094
91722926017229261G37GENIChomozygous128685095
91722926417229264A35GENIChomozygous128685096
91722927117229272TC32GENIChomozygous128766714
91722927217229273CT32GENIChomozygous128766715
91722927517229276G32GENIChomozygous128685097
91722927917229280C32GENIChomozygous128685098
91722928717229287T36GENIChomozygous128685099
91722929017229291GA36GENIChomozygous117270252
91722930217229302G37GENIChomozygous128685100
91722930817229309A42GENIChomozygous128685101
91722932517229327CA44GENIChomozygous128685102
91722934117229342C42GENIChomozygous128685103
91722937517229375T36GENIChomozygous130676277
91722938417229384G35GENIChomozygous130676278
91722940617229407C33GENIChomozygous130676279
91723027717230278G10GENIChomozygous128685104
91723027917230281CA10GENIChomozygous128685105
91723033717230339CC18GENIChomozygous128685106
91723035217230352C19GENIChomozygous128685107
91723038517230386T23GENIChomozygous128685108
91723038817230388A24GENIChomozygous128685109
91723042517230426G32GENIChomozygous128685110
91723048817230488GA28GENIChomozygous128685111
91723050317230504T24GENICpossibly homozygous128685112
91723322017233221CT50GENIChomozygous117270253
91723323117233232CG47GENIChomozygous117270254
91723326817233269AG48GENIChomozygous117270255