chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144502247144502248TG17GENIChomozygous114650322
5144504817144504818GA13GENIChomozygous114037351
5144506688144506689TC22GENIChomozygous114037354
5144509949144509950GT11GENICpossibly homozygous114037357
5144509987144509988TG17GENICpossibly homozygous114650324
5144510054144510055TC26GENIChomozygous114037358
5144510251144510252GC9GENIChomozygous114152413
5144512971144512972TG19GENIChomozygous114037359
5144513243144513244GA15GENIChomozygous114037360
5144513656144513657TC26GENIChomozygous114037361
5144513864144513865CT17GENIChomozygous114650326
5144516413144516414AG17GENIChomozygous114650328
5144523965144523966AC35GENIChomozygous114037371
5144527949144527950CT25GENIChomozygous114650330
5144528518144528519AT16GENIChomozygous114037374
5144537865144537866GC6GENIChomozygous114037376
5144537869144537870TC4GENIChomozygous114037377
5144539354144539355AG21GENIChomozygous114037384
5144542451144542452AG18GENIChomozygous114037385
5144542669144542670TC12GENIChomozygous114650334
5144542721144542722GT2GENIChomozygous114681805
5144542840144542841TC9GENIChomozygous114650338
5144547230144547231GA14GENICpossibly homozygous114650340
5144547260144547261GA18GENICheterozygous114650342
5144548783144548784GA23GENIChomozygous114650344
5144552469144552470GC23GENIChomozygous114037401
5144552557144552558GA3GENIChomozygous114037402
5144552577144552578TC3GENIChomozygous114037403
5144552993144552994CT18GENIChomozygous114037404
5144553033144553034TC17GENIChomozygous114037405
5144553351144553352CT34GENIChomozygous114037406
5144553996144553997GT30GENIChomozygous114037407
5144554514144554515AG18GENIChomozygous114037408
5144554721144554722AG20GENIChomozygous114650346
5144554784144554785CT15GENIChomozygous114037409
5144554991144554992GA10GENIChomozygous114650348
5144556630144556631CT19GENIChomozygous114037412
5144556660144556661TG21GENIChomozygous114037413