chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91722796217227962C30GENIChomozygous128685083
91722805317228053T34GENIChomozygous128685084
91722806117228064CCT34GENIChomozygous128685085
91722909417229095G42GENIChomozygous128685086
91722910817229108G42GENIChomozygous128685087
91722911617229117TG44GENIChomozygous117682184
91722911717229118GT45GENIChomozygous117682186
91722912617229127T42GENIChomozygous128685088
91722913117229131T43GENIChomozygous128685089
91722919417229194G44GENIChomozygous128685090
91722919617229197T43GENIChomozygous128685091
91722920417229206TC47GENIChomozygous128685092
91722922917229230T45GENIChomozygous128685093
91722925317229254A48GENIChomozygous128685094
91722926017229261G50GENIChomozygous128685095
91722926417229264A50GENIChomozygous128685096
91722927117229272TC50GENIChomozygous128766714
91722927217229273CT51GENIChomozygous128766715
91722927517229276G50GENIChomozygous128685097
91722927917229280C50GENIChomozygous128685098
91722928717229287T51GENIChomozygous128685099
91722929017229291GA50GENIChomozygous117270252
91722930217229302G48GENIChomozygous128685100
91722930817229309A48GENIChomozygous128685101
91722932517229327CA48GENIChomozygous128685102
91722934117229342C49GENIChomozygous128685103
91723027717230278G28GENIChomozygous128685104
91723027917230281CA28GENIChomozygous128685105
91723033717230339CC25GENIChomozygous128685106
91723035217230352C27GENIChomozygous128685107
91723038517230386T33GENIChomozygous128685108
91723038817230388A33GENIChomozygous128685109
91723042517230426G42GENIChomozygous128685110
91723048817230488GA32GENIChomozygous128685111
91723050317230504T29GENIChomozygous128685112
91723322017233221CT25GENIChomozygous117270253
91723323117233232CG23GENIChomozygous117270254
91723326817233269AG28GENIChomozygous117270255