chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124794761747947618AG22GENICpossibly homozygous115345109
124795012347950124GA32GENIChomozygous115345111
124795043147950432AT32GENIChomozygous115345113
124795345447953455GT27GENIChomozygous115345115
124795356947953570GT21GENIChomozygous115398715
124795378647953787TG24GENIChomozygous115345117
124795389047953891GT25GENIChomozygous115345119
124795397347953974TG23GENIChomozygous115345121
124795397847953979GC23GENIChomozygous115345123
124795417447954175CG25GENIChomozygous115430463
124795681847956819TC15GENIChomozygous115345127
124796635847966359CG36GENIChomozygous115345135
124796503347965034CT27GENIChomozygous115345131
124796588147965882CT20GENIChomozygous115345133
124796935247969353CG13GENIChomozygous115345137
124797145347971454GA25GENIChomozygous115345139
124797146247971463GT23GENIChomozygous115345141
124797233747972338TG30GENIChomozygous115345143
124797846947978470TC28GENIChomozygous115345145
124797921947979220GA21GENIChomozygous115345147
124798207847982079TC29GENIChomozygous115345149
124798222647982227CT20GENICpossibly homozygous115345151
124798261447982615CA22GENIChomozygous115345153
124798623747986238TC25GENIChomozygous115345155
124798625847986259TC21GENIChomozygous115345157
124798787847987879AG23GENIChomozygous115345159
124798995147989952AT5GENIChomozygous115345161
124799121347991214GT35GENIChomozygous115398801
124799121947991220CA30GENIChomozygous115345165