chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103658721536587216CT18GENIChomozygous116561321
103658743036587431TC19GENICpossibly homozygous116561323
103658743936587440TC18GENIChomozygous116561325
103658898536588986GA11GENIChomozygous116561329
103659045336590454AG22GENIChomozygous116561331
103659066136590662GA23GENIChomozygous116561333
103659291436592915CG19GENIChomozygous116561335
103659360136593602AT23GENIChomozygous116561337
103659389836593899TC27GENIChomozygous116561339
103659609936596100GA22GENIChomozygous116561341
103659672236596723CT13GENIChomozygous116561343
103659694536596946CT16GENIChomozygous116561345
103659699636596997CT10GENIChomozygous116561347
103659785736597858GA33GENICpossibly homozygous116561349