chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74475193344751933A59GENIChomozygous128460125
74475247644752477TC67GENIChomozygous115665716
74475431844754319TA67GENIChomozygous115665720
74475432444754325A68GENIChomozygous131013311
74475582044755821GC46GENIChomozygous115665724
74475651444756515TC59GENIChomozygous116154524
74475665644756657CT56GENIChomozygous115665728
74475743844757439CT43GENICpossibly homozygous116154526
74475782444757825TC51GENIChomozygous115665734
74475788444757884TAA52GENIChomozygous128460127
74475578444755790AACTTT48GENIChomozygous131013312
74475648944756489TT53GENIChomozygous131013313
74475814044758141GA77GENIChomozygous116154528
74475874544758746TA59GENIChomozygous115665747
74475877144758772AG56GENIChomozygous116154530
74475883944758840GA65GENIChomozygous116154532
74475901144759012AG58GENIChomozygous116154534
74475944844759448A50GENICpossibly homozygous131013314
74475964344759644CT30GENIChomozygous116154536
74476061944760620AG57GENIChomozygous115665759
74476083544760836TA60GENIChomozygous116154538
74476244844762449TG57GENIChomozygous115665773
74476265244762654TC30GENIChomozygous131013315
74476265744762658GC30GENIChomozygous122767972
74476271044762711AG56GENIChomozygous116154542
74476285944762860TC58GENIChomozygous116154544
74476320444763205AG80GENIChomozygous115665779
74476364644763647GA75GENIChomozygous116154546
74476409844764099A63GENIChomozygous131013316
74476431744764317T50GENIChomozygous131013317
74476484844764849GA66GENIChomozygous116154548
74476700144767005ATAT53GENIChomozygous128460135
74476818844768189CT63GENIChomozygous116154550
74476822044768221GA61GENIChomozygous116154552
74476834644768347TC61GENIChomozygous115665792
74476848944768489A37GENIChomozygous128460136
74476882044768829GTGTGGGGA15GENIChomozygous128460137
74476905944769060AT58GENIChomozygous115665796
74476938044769381AG63GENIChomozygous115665798
74477035444770363GACATCCAG47GENIChomozygous131013318
74477049044770491TG84GENIChomozygous115665802
74477104244771043GT59GENICpossibly homozygous115665804