chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38131501781315018AT7GENICheterozygous112133170
38131639081316391GA11GENIChomozygous111636450
38131816481318165GA18GENIChomozygous111636451
38132172581321726TG6GENIChomozygous111636452
38132194281321943AG20GENIChomozygous111636453
38132330581323306GT6GENIChomozygous111636454
38132414881324149AG18GENIChomozygous111636455
38132445281324453AG14GENIChomozygous111636456
38132505281325053TC14GENIChomozygous111636457
38132510881325109AG25GENIChomozygous111636458
38132691681326917GA10GENIChomozygous111636459
38132729781327298GC14GENIChomozygous111636460
38132829581328296AG16GENIChomozygous111636461
38132856681328567CT8GENIChomozygous111636463
38132962481329625AT15GENIChomozygous111636466
38133631881336319GC14GENIChomozygous111636467
38133700381337004TC11GENIChomozygous111636468
38133728981337290TA23GENIChomozygous111636469
38133970081339701TC9GENIChomozygous111636470
38134130881341309CG6GENIChomozygous111636471
38134173581341736GA19GENIChomozygous111636472
38134188581341886CT10GENICheterozygous111636473
38134346281343463AG16GENIChomozygous111636474
38134348581343486AC18GENIChomozygous111636475
38133824981338250TG5GENIChomozygous125827337