chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106566568965665690CT7GENIChomozygous116793169
106566668865666689TC10GENIChomozygous116793171
106566960465669605AG25GENIChomozygous116793173
106567411865674119GA8GENIChomozygous116793175
106567412565674126CG8GENIChomozygous116619195
106567467665674677TC7GENIChomozygous116619197
106567643265676433CT14GENIChomozygous116793177
106567648865676489GT17GENIChomozygous116619199
106567859565678596GA12GENIChomozygous116793179
106567862065678621AC15GENIChomozygous116619203
106567877365678774AG17GENIChomozygous116793181
106567900465679005GT22GENIChomozygous116793183
106568271865682719GC9GENIChomozygous126385185
106568272565682726TC6GENIChomozygous126385186
106568274365682744AC11GENIChomozygous126409495
106568278765682788AT4GENIChomozygous116793185
106568298765682988CT19GENIChomozygous116793189
106568355165683552GA16GENIChomozygous116619211
106568387665683877GA22GENIChomozygous116793191
106568506765685068GA13GENIChomozygous116793193
106568514465685145CA12GENIChomozygous116793195
106568565365685654GA12GENIChomozygous116619215
106568597865685979CT18GENIChomozygous116793197
106568603665686037TC9GENIChomozygous117130927
106568683765686838CT16GENICheterozygous116793199
106568692365686924CT13GENIChomozygous116619217
106568710065687101TC15GENIChomozygous116619221
106568733265687333CT11GENIChomozygous116619223
106568806965688070CT15GENIChomozygous116793201
106568896265688963CA14GENIChomozygous116793203
106568973565689736GT18GENIChomozygous116793205
106569047065690471TA15GENIChomozygous116619235