chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2031761633176164AG50GENIChomozygous109068219
2031776273177628AT55GENICpossibly homozygous109068221
2031790723179073AG53GENIChomozygous109068223
2031791403179141TC46GENIChomozygous109068225
2031801083180109AG35GENIChomozygous109068227
2031808063180807TC69GENIChomozygous109576016
2031807383180739T60GENIChomozygous129650636
2031807723180773TC73GENIChomozygous119755920
2031807873180788GA72GENIChomozygous119755921
2031807903180791AG72GENIChomozygous119755922
2031807923180793AC71GENIChomozygous119755923