chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186229130562291306TC38GENIChomozygous110376759
186229135462291355GC35GENIChomozygous110376761
186229152262291523TG31GENIChomozygous110376763
186229186362291864AG25GENIChomozygous110483571
186229209962292100TG40GENICpossibly homozygous110376765
186229215662292157AG35GENIChomozygous110483573
186229278362292784TC27GENICheterozygous119563241
186229320462293205CG27GENIChomozygous110376771
186229357962293580CA18GENIChomozygous110376775
186230202262302023GA11GENIChomozygous119554366
186230269162302692CT12GENIChomozygous119497270
186230275362302754GA8GENIChomozygous119497273
186230423462304235AG24GENIChomozygous110376882
186230598062305981TC27GENIChomozygous110376904
186230945662309457TC11GENICpossibly homozygous110483577
186230930862309309CG11GENIChomozygous110815659