chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38131501781315018AT15GENICpossibly homozygous112133170
38131502181315022AT15GENIChomozygous111636449
38131639081316391GA27GENIChomozygous111636450
38131816481318165GA22GENIChomozygous111636451
38131914581319146CT19GENIChomozygous112133172
38132172581321726TG14GENIChomozygous111636452
38132194281321943AG24GENIChomozygous111636453
38132330581323306GT18GENIChomozygous111636454
38132414881324149AG22GENIChomozygous111636455
38132445281324453AG19GENIChomozygous111636456
38132505281325053TC24GENIChomozygous111636457
38132510881325109AG30GENIChomozygous111636458
38132691681326917GA27GENIChomozygous111636459
38132729781327298GC16GENIChomozygous111636460
38132829581328296AG19GENIChomozygous111636461
38132856681328567CT22GENIChomozygous111636463
38132877881328779CT25GENIChomozygous111636464
38132948381329484GA5GENIChomozygous111636465
38132962481329625AT12GENIChomozygous111636466
38133631881336319GC26GENIChomozygous111636467
38133700381337004TC19GENIChomozygous111636468
38133728981337290TA32GENIChomozygous111636469
38133970081339701TC24GENIChomozygous111636470
38134130881341309CG15GENIChomozygous111636471
38134173581341736GA30GENIChomozygous111636472
38134188581341886CT40GENIChomozygous111636473
38134346281343463AG12GENIChomozygous111636474
38134348581343486AC15GENIChomozygous111636475