chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153878787938787880CG21GENIChomozygous112481069
153878788638787887CG18GENIChomozygous112481071
153878789238787893CA20GENIChomozygous112481073
153878789938787900CT17GENIChomozygous112481075
153878790238787903CA18GENIChomozygous112481077
153878790638787907CT17GENIChomozygous112481079
153878791038787911CT18GENIChomozygous112481081
153880247538802476AT29GENIChomozygous112481142
153880248538802486GT30GENIChomozygous112481144
153882103238821033AT5GENIChomozygous113097318
153885716338857164AG9GENIChomozygous112672763
153893214038932141TG21GENIChomozygous112988109
153900761639007617GC27GENIChomozygous112672774
153900788339007884GT22GENIChomozygous112481905
153900852739008528AT17GENIChomozygous112672776
153900852839008529TA17GENIChomozygous112481907
153900883239008833TA10GENIChomozygous112481909
153900883739008838AT10GENIChomozygous112481911
153900883839008839TA10GENIChomozygous112481913
153901522339015224TC17GENIChomozygous112481921
153902707839027079AC24GENIChomozygous112482009
153908421839084219TC10GENIChomozygous113079197
153908424539084246TA7GENIChomozygous113169256
153908425339084254GT7GENIChomozygous113097322
153908425439084255TG7GENIChomozygous113097324
153915853139158532CA28GENIChomozygous112482536
153917929539179296TC5GENIChomozygous112988111
153926627039266271CA20GENIChomozygous112672792
153934201539342016AG2GENIChomozygous113000549
153934201739342018AG2GENIChomozygous113000551
153937069439370695GT11GENIChomozygous112483291
153938557939385580TG20GENIChomozygous112672822
153945592439455925AT11GENIChomozygous112808110
153945598239455983AT13GENIChomozygous112483434
153946700039467001AC28GENIChomozygous112483450
153946703239467033AT27GENIChomozygous112483453
153963533039635331CT3GENIChomozygous112672826
153963533139635332GA3GENIChomozygous112483805
153964076439640765TG23GENIChomozygous112672830
153965245839652459GA22GENIChomozygous113053342