chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144102304144102305GA29GENICheterozygous812724136
7144102372144102373CG85GENICheterozygous812724137
7144102432144102433GC77GENICheterozygous812724138
7144102434144102435TC75GENICheterozygous812724139
7144102435144102436TA75GENICheterozygous812724140
7144102441144102442CG81GENICheterozygous812724141
7144102468144102469TC79GENICheterozygous812724142
7144102475144102476TC77GENICheterozygous812724143
7144102479144102480GT78GENICheterozygous812724144
7144102494144102495AC68GENICheterozygous812724145
7144102500144102501CG68GENICheterozygous812724146
7144102526144102527TC60GENICheterozygous812724147
7144102592144102593AG57GENICheterozygous812724148
7144102622144102623CT67GENICheterozygous812724149
7144102716144102717AC85GENICpossibly homozygous812724150
7144102722144102723GT86GENICpossibly homozygous812724151
7144102744144102745CA89GENICpossibly homozygous812724152
7144102784144102785CG85GENICheterozygous812724153
7144102837144102838GA80GENICheterozygous812724154
7144102851144102852GA76GENICheterozygous812724155
7144102856144102857TG74GENICheterozygous812724156
7144102888144102889CT52GENICheterozygous812724157
7144102889144102890AT52GENICheterozygous812724158
7144102894144102895CA51GENICheterozygous812724159
7144102921144102922TC35GENICheterozygous812724160
7144104831144104832GA37GENIChomozygous812724161
7144105165144105166TG17GENIChomozygous812724162
7144106013144106014TA37GENIChomozygous812724163
7144106223144106224AC25GENIChomozygous812724164
7144107661144107662AG34GENIChomozygous812724165
7144107952144107953CT22GENIChomozygous812724166
7144109598144109599CG45GENIChomozygous812724167
7144109611144109612CT40GENIChomozygous812724168
7144110822144110823CT31GENIChomozygous812724169
7144112570144112571TC33GENIChomozygous812724170
7144115720144115721GA32GENIChomozygous812724171
7144117356144117357CT44GENIChomozygous812724172
7144119226144119227CT37GENIChomozygous812724173