chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74475193344751933A14GENIChomozygous128460125
74475247644752477TC13GENIChomozygous115665716
74475431844754319TA14GENIChomozygous115665720
74475582044755821GC12GENIChomozygous115665724
74475665644756657CT17GENIChomozygous115665728
74475782444757825TC14GENIChomozygous115665734
74475788444757884TAA13GENIChomozygous128460127
74475901144759012AG15GENIChomozygous116154534
74475874544758746TA12GENIChomozygous115665747
74475432444754325A15GENIChomozygous131013311
74475578444755790AACTTT14GENIChomozygous131013312
74475648944756489TT24GENIChomozygous131013313
74475651444756515TC28GENIChomozygous116154524
74475743844757439CT6GENIChomozygous116154526
74475814044758141GA21GENIChomozygous116154528
74475877144758772AG11GENIChomozygous116154530
74475883944758840GA15GENIChomozygous116154532
74475944844759448A15GENIChomozygous131013314
74475964344759644CT18GENIChomozygous116154536
74476061944760620AG12GENIChomozygous115665759
74476083544760836TA15GENIChomozygous116154538
74476244844762449TG20GENIChomozygous115665773
74476265244762654TC7GENIChomozygous131013315
74476265744762658GC7GENIChomozygous122767972
74476271044762711AG16GENIChomozygous116154542
74476285944762860TC19GENIChomozygous116154544
74476320444763205AG17GENIChomozygous115665779
74476364644763647GA22GENIChomozygous116154546
74476409844764099A17GENIChomozygous131013316
74476431744764317T21GENIChomozygous131013317
74476484844764849GA15GENIChomozygous116154548
74476700144767005ATAT12GENIChomozygous128460135
74476818844768189CT13GENIChomozygous116154550
74476822044768221GA12GENIChomozygous116154552
74476834644768347TC13GENIChomozygous115665792
74476848944768489A14GENICpossibly homozygous128460136
74476905944769060AT17GENIChomozygous115665796
74476938044769381AG10GENIChomozygous115665798
74477035444770363GACATCCAG16GENIChomozygous131013318
74477049044770491TG15GENIChomozygous115665802
74477104244771043GT12GENIChomozygous115665804