chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
192502912525029125C14GENIChomozygous129595696
192502914125029142G14GENIChomozygous129595697
192502916325029163GGC11GENIChomozygous129595698
192502917325029174G10GENIChomozygous129595699
192502917825029179C10GENIChomozygous129595700
192502918225029183GC9GENIChomozygous109672124
192502920425029204C10GENIChomozygous129595701
192502926825029269G11GENIChomozygous129595702
192502928725029288AG13GENIChomozygous109672126
192502931325029313G12GENIChomozygous129595703
192502932425029326GT12GENIChomozygous129595704
192502934725029347G12GENIChomozygous129595705
192502938025029380C12GENIChomozygous129595706
192502940125029402G10GENIChomozygous129595707
192502941125029411G9GENIChomozygous129595708
192502942225029422G11GENIChomozygous129595709
192502944525029445C10GENIChomozygous129595710
192502945725029457C12GENIChomozygous129595711
192502945925029460G12GENIChomozygous129595712
192503692125036922AG16GENIChomozygous109672132
192503911725039118CA5GENIChomozygous109672134
192504257125042572AG17GENIChomozygous109672140
192504455325044554TC8GENIChomozygous109672144
192504612025046120TG21GENIChomozygous129595713
192504672625046727CT17GENIChomozygous109866738
192504075925040760GA15GENIChomozygous131222918
192504287725042878CT16GENIChomozygous131222919
192504787125047872CT18GENIChomozygous109866740
192505437925054380CT12GENIChomozygous109672154
192506109125061092GA18GENIChomozygous131222920
192506207625062077AG21GENIChomozygous109672156
192506517325065174TC14GENIChomozygous109672160
192506550325065504TC19GENIChomozygous109672164
192506648825066489G11GENIChomozygous129595717
192506873325068734AG15GENIChomozygous131222921
192506705125067066GCCCCAGGCTGGGAG12GENIChomozygous131217322