chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5130394077130394078AG23GENICheterozygous55717484
5130400230130400231TC20GENICheterozygous55717496
5130405636130405639TTT---28GENICheterozygous56573503
5130405637130405639TT--28GENICheterozygous56450769
5130416069130416070GA22GENICheterozygous56894408
5130420652130420653TC31GENICheterozygous56894414
5130421428130421429TC17GENICheterozygous56894426
5130428482130428483AC16GENICheterozygous55717582
5130428494130428495GT19GENICheterozygous56894440
5130429206130429207CT36GENICheterozygous55717584
5130429990130429991CT30GENICheterozygous56894442
5130430014130430015CT30GENICheterozygous55717588
5130430028130430029GA29GENICheterozygous56894444
5130430040130430041CT29GENICheterozygous55717590
5130431983130431984TG6GENICheterozygous55717602
5130435082130435083AG16GENICheterozygous55717616
5130440750130440751CG18GENICheterozygous56655924
5130446565130446566CG13GENICheterozygous55717662
5130448314130448315GA13GENICheterozygous56894450
5130452471130452472CT19GENICheterozygous56185868
5130476762130476763AAT58GENICheterozygous55717756
5130476800130476801G-83GENICheterozygous55717758
5130482841130482842C-11GENICheterozygous56894453
5130488006130488007AT27GENICheterozygous55717783
5130490057130490058TC15GENICheterozygous56185936
5130490780130490781AC5GENICheterozygous56185941
5130491390130491391CA35GENICheterozygous56185943