chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105531507055315071AG26GENICpossibly homozygous51889635
105531551755315518AG14GENIChomozygous51652722
105531570755315708T-4GENIChomozygous51652726
105531587155315872AG7GENIChomozygous51652728
105531611155316112A-3GENIChomozygous51889638
105531678955316790GA20GENICheterozygous51889641
105531860055318601AG16GENICheterozygous51889644
105531860155318602CT17GENICheterozygous51459396
105531907955319080AT17GENIChomozygous51459397
105531935955319360GA13GENICpossibly homozygous51889647
105531936355319364GGGA12GENIChomozygous51652732
105532038955320390GA11GENIChomozygous51889649
105532082055320821AG4GENIChomozygous51459398
105532282255322823AAAAGCAAAGCAACAT4GENICheterozygous51459400
105532422055324221AC4GENIChomozygous51459403
105532585855325859TC18GENICpossibly homozygous51459404
105532628755326288AG12GENICheterozygous51459405
105532766455327836TAAGCTGCTGTCTCTTTTTTTTTTTTTTTGGGTTCTTTTTTTTTTTTTTTTTTTACTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC----------------------------------------------------------------------------------------------------------------------------------------------------------------------------13GENICheterozygous52319022
105532798655327987GGGGGCGGGTAGTGAGTGT1GENIChomozygous52319024
105532800355328004AG1GENIChomozygous51459407
105532941555329416AG20GENIChomozygous51459409
105533043855330439TC19GENIChomozygous51459410
105533230155332302AAGAG6GENIChomozygous51459414
105533323355333234CT8GENICheterozygous51459415
105533581655335817CT17GENIChomozygous51459419