chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17877202878772029CT16GENICpossibly homozygous108873063
17877625978776260CT12GENIChomozygous120839239
17877942478779425TC27GENIChomozygous108873068
17877959278779593TC20GENIChomozygous108873069
17878199378781994TC27GENIChomozygous108873070
17878518478785185AG43GENIChomozygous108873074
17878659978786600GA25GENICpossibly homozygous120839240
17878807178788072CT32GENIChomozygous120839241
17879310878793109TG26GENIChomozygous108873079
17879494778794948GA16GENIChomozygous108873080
17879605878796059TC34GENICpossibly homozygous108873081