chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102136316102136317G-5GENIChomozygous51587352
10102137007102137008TC28GENIChomozygous51587354
10102137511102137512AG51GENIChomozygous51587356
10102137788102137789GA27GENIChomozygous51587358
10102137857102137858TC30GENIChomozygous51587360
10102137865102137866AG31GENIChomozygous51587362
10102138327102138328AG24GENIChomozygous51587364
10102139127102139128GA29GENIChomozygous51587366
10102139449102139450TC23GENIChomozygous51587368
10102139634102139635AT14GENIChomozygous51587370
10102139666102139669TTC---18GENIChomozygous51587374
10102139770102139771CT20GENIChomozygous51587376
10102140038102140039CT34GENIChomozygous51587378
10102140142102140143CCACACAGAG2GENIChomozygous52403770
10102140505102140506TC22GENIChomozygous51587380
10102141647102141648AG28GENIChomozygous51587382
10102141652102141653AG27GENIChomozygous51587384
10102141692102141693CA26GENIChomozygous51587386
10102141972102141973T-22GENIChomozygous51587388
10102142112102142113TTG19GENIChomozygous51587390
10102142276102142277TC33GENIChomozygous51587392
10102143189102143190CCAAA10GENICheterozygous51587396