chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74475193344751933A40GENICpossibly homozygous128460125
74475247644752477TC45GENIChomozygous115665716
74475431844754319TA49GENIChomozygous115665720
74475432444754325A46GENIChomozygous131013311
74475578444755790AACTTT45GENIChomozygous131013312
74475582044755821GC47GENIChomozygous115665724
74475648944756489TT39GENIChomozygous131013313
74475665644756657CT42GENIChomozygous115665728
74475782444757825TC42GENIChomozygous115665734
74475788444757884TAA49GENIChomozygous128460127
74475874544758746TA45GENIChomozygous115665747
74475877144758772AG42GENIChomozygous116154530
74475651444756515TC49GENIChomozygous116154524
74475743844757439CT34GENIChomozygous116154526
74475814044758141GA57GENIChomozygous116154528
74475883944758840GA42GENIChomozygous116154532
74475901144759012AG61GENIChomozygous116154534
74475944844759448A47GENIChomozygous131013314
74475964344759644CT27GENIChomozygous116154536
74476061944760620AG44GENIChomozygous115665759
74476083544760836TA52GENIChomozygous116154538
74476244844762449TG59GENIChomozygous115665773
74476265244762654TC32GENIChomozygous131013315
74476265744762658GC32GENIChomozygous122767972
74476271044762711AG47GENIChomozygous116154542
74476285944762860TC44GENIChomozygous116154544
74476320444763205AG52GENIChomozygous115665779
74476364644763647GA46GENIChomozygous116154546
74476409844764099A41GENIChomozygous131013316
74476431744764317T51GENIChomozygous131013317
74476484844764849GA46GENIChomozygous116154548
74476700144767005ATAT38GENIChomozygous128460135
74476818844768189CT42GENIChomozygous116154550
74476822044768221GA41GENIChomozygous116154552
74476834644768347TC42GENIChomozygous115665792
74476848944768489A30GENICpossibly homozygous128460136
74476882044768829GTGTGGGGA14GENIChomozygous128460137
74476905944769060AT44GENIChomozygous115665796
74476938044769381AG50GENIChomozygous115665798
74477035444770363GACATCCAG49GENIChomozygous131013318
74477049044770491TG54GENICpossibly homozygous115665802
74477104244771043GT51GENIChomozygous115665804