chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5119049938119049939CT8GENICheterozygous595517606
5119050135119050136TC6GENIChomozygous597387187
5119054319119054320GA16GENIChomozygous595517607
5119054330119054331CT15GENICpossibly homozygous597387188
5119054761119054762TG19GENICpossibly homozygous595517608
5119055350119055351A-3GENIChomozygous727081237
5119055369119055370GA16GENIChomozygous597387189
5119056193119056194AG31GENICpossibly homozygous597387190
5119058417119058418GA21GENICpossibly homozygous595517609
5119060466119060467CT35GENIChomozygous597387191
5119061102119061103AC16GENICpossibly homozygous597387192
5119067159119067160TC12GENIChomozygous595517610
5119069262119069263CT10GENIChomozygous597387193
5119069269119069270GT11GENIChomozygous597387194