chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130470704130470705G38GENIChomozygous137341382
5130472926130472927T41GENICpossibly homozygous137341383
5130474901130474902AG57GENIChomozygous137621184
5130475743130475743GGAGAGGGAGAC47GENIChomozygous137341384
5130476186130476187AG57GENIChomozygous137621185
5130477513130477514AG45GENICpossibly homozygous137621186
5130478246130478247TC61GENIChomozygous137621187
5130479680130479681AG60GENIChomozygous137621188
5130479750130479751GA50GENIChomozygous137621189