chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105620389756203898AG19GENIChomozygous51654670
105620401256204013AG14GENIChomozygous51654672
105620401856204019AG14GENIChomozygous51654674
105620438756204388AG8GENIChomozygous51654676
105620446356204464AG16GENIChomozygous51654678
105620609456206095CT16GENIChomozygous51891265
105620697356206974TG20GENIChomozygous51654688
105620711756207118GGC14GENIChomozygous51460011
105620712756207133TCTTAT------12GENIChomozygous52377699
105620713356207134GGAGA10GENIChomozygous52377702
105620713556207136GC9GENIChomozygous51460014
105620835456208355AG12GENIChomozygous51654696
105620881756208818TC7GENIChomozygous51654698
105620917956209180TC17GENIChomozygous51654700
105620964456209645GA29GENIChomozygous51891268
105620970556209706AAGAAG19GENIChomozygous51654702
105620989256209893AG26GENIChomozygous51654704
105621119756211198TTACACACACACAC3GENICheterozygous52502466
105621163056211631GA23GENIChomozygous51891274