chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274651771274651772CG38GENIChomozygous965902697
1274657810274657811TC42GENICpossibly homozygous965902698
1274659225274659226AC19GENIChomozygous965902699
1274659241274659242CG19GENIChomozygous965902700
1274660485274660486AG38GENIChomozygous965902701