chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130470704130470705G23GENIChomozygous137341382
5130471437130471438CG29GENIChomozygous143959765
5130474249130474250GA25GENIChomozygous143959766
5130475743130475743GGAGAGGGAGAC16GENIChomozygous137341384
5130478037130478038GT18GENIChomozygous143959767
5130478246130478247TC11GENIChomozygous137621187
5130473591130473591A14GENICpossibly homozygous143943810
5130477354130477362CACACACG15GENIChomozygous143943811
5130477383130477389GCACGC16GENIChomozygous143943812
5130474901130474902AG20GENIChomozygous137621184
5130476186130476187AG16GENIChomozygous137621185
5130477513130477514AG20GENIChomozygous137621186