chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2216154858216154859CCA25GENIChomozygous59391828
2216155534216155542TGTGTGTG--------8GENICpossibly homozygous60516873
2216156893216156894TTG7GENIChomozygous59391830
2216156945216156946CT8GENIChomozygous59391833
2216156973216156974GA7GENIChomozygous59391834
2216157599216157600CG29GENIChomozygous59391835
2216158440216158441GA27GENIChomozygous59391836
2216158588216158589GA20GENIChomozygous59391837
2216159146216159147CCT11GENICheterozygous59391841
2216159854216159855GC25GENIChomozygous59391842
2216160282216160283CT18GENIChomozygous59391843
2216160479216160483GTGT----4GENIChomozygous60516876
2216161196216161197TG13GENIChomozygous59391845
2216164111216164112TC18GENIChomozygous59391846
2216164217216164218TTACAC3GENICheterozygous59391847