chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA28GENIChomozygous951543134
1263813164263813165CA29GENICpossibly homozygous951543135
1263813314263813315GA30GENIChomozygous951543136
1263813492263813493TA30GENICpossibly homozygous951543137
1263814051263814052CT25GENIChomozygous951543138
1263815349263815350GA16GENIChomozygous951543139
1263815744263815745AG38GENIChomozygous951543140
1263817743263817744AG28GENIChomozygous951543141
1263820813263820814AG36GENIChomozygous951543142
1263820861263820862CT23GENIChomozygous951543143
1263821401263821402GA31GENIChomozygous951543144
1263823231263823232GA45GENIChomozygous951543145
1263823243263823244CT43GENIChomozygous951543146
1263823512263823513AG37GENIChomozygous951543147
1263825765263825766GT31GENIChomozygous951543148
1263827331263827332GA19GENIChomozygous951543149
1263828502263828503CA29GENIChomozygous951543150
1263831722263831723CT26GENIChomozygous951543151
1263832115263832116TC30GENIChomozygous951543152
1263832813263832814AG18GENIChomozygous951543153
1263835278263835279CT35GENIChomozygous951543154
1263835926263835927GA24GENIChomozygous951543155
1263837493263837494GA21GENIChomozygous951543156
1263840846263840847CT35GENIChomozygous951543157
1263842282263842283GT27GENIChomozygous951543158
1263843300263843301AT34GENIChomozygous951543159
1263844963263844964AG21GENIChomozygous951543160