chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106566668865666689TC12GENIChomozygous116793171
106566960465669605AG21GENIChomozygous116793173
106567100965671010CA5GENICheterozygous126422457
106567411865674119GA7GENIChomozygous116793175
106567643265676433CT16GENIChomozygous116793177
106567412565674126CG9GENIChomozygous116619195
106567467665674677TC11GENIChomozygous116619197
106567648865676489GT16GENIChomozygous116619199
106567859565678596GA13GENIChomozygous116793179
106567862065678621AC9GENIChomozygous116619203
106567877365678774AG12GENIChomozygous116793181
106567900465679005GT21GENIChomozygous116793183
106568271865682719GC9GENIChomozygous126385185
106568272565682726TC5GENIChomozygous126385186
106568274365682744AC9GENIChomozygous126409495
106568298765682988CT20GENIChomozygous116793189
106568355165683552GA9GENIChomozygous116619211
106568387665683877GA28GENIChomozygous116793191
106568506765685068GA4GENIChomozygous116793193
106568514465685145CA8GENIChomozygous116793195
106568565365685654GA5GENIChomozygous116619215
106568597865685979CT15GENIChomozygous116793197
106568683765686838CT9GENIChomozygous116793199
106568692365686924CT12GENIChomozygous116619217
106568710065687101TC14GENIChomozygous116619221
106568733265687333CT11GENIChomozygous116619223
106568798965687990AC14GENIChomozygous116619225
106568806965688070CT17GENIChomozygous116793201
106568896265688963CA9GENIChomozygous116793203
106568969665689697CT14GENIChomozygous116619227
106568969965689700AG13GENIChomozygous116619229
106568973565689736GT24GENIChomozygous116793205
106569047065690471TA10GENIChomozygous116619235