chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118685259118685260GA16GENIChomozygous886696177
7118685585118685586GA18GENIChomozygous886696178
7118686769118686770CT14GENIChomozygous886696179
7118686787118686788TC10GENIChomozygous886696180
7118686827118686828TA10GENIChomozygous886696181
7118686951118686952AG7GENIChomozygous886696182
7118686953118686954AG4GENICheterozygous886696183
7118688724118688725GT6GENIChomozygous886696184
7118688732118688733TG7GENIChomozygous886696185
7118688886118688887TG15GENICheterozygous886696186
7118689200118689201AG18GENIChomozygous886696187
7118689643118689644CT7GENICheterozygous886696188
7118690139118690140GA15GENICheterozygous886696189
7118690472118690473GA9GENIChomozygous886695986
7118690475118690476GA6GENICheterozygous886696190
7118690797118690798CT19GENICheterozygous886696191
7118691912118691913CT17GENIChomozygous886695985
7118692035118692036TC23GENIChomozygous886696192
7118692062118692063GA12GENICheterozygous886696193
7118692156118692157TC16GENIChomozygous886696194
7118692446118692447CT15GENIChomozygous886696195
7118692627118692628TC9GENICheterozygous886696196
7118693744118693745GA9GENIChomozygous886696197
7118693894118693895CA18GENICheterozygous886696198