chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154503063154503064T-7GENIChomozygous55803586
5154503115154503116GC14GENIChomozygous55803587
5154503126154503127GC14GENIChomozygous55803588
5154503144154503145GT16GENIChomozygous55803589
5154503146154503147GT16GENIChomozygous55803590
5154504000154504001T-7GENICheterozygous56554581
5154524133154524134CCAA2GENICheterozygous56532942
5154524134154524135A-2GENICheterozygous55803593
5154551972154551973A-6GENICheterozygous56554582
5154557493154557494T-9GENICheterozygous56554583
5154559541154559542T-15GENICheterozygous56070854
5154563616154563622GTGTGT------10GENICheterozygous56554584
5154566458154566459TTATAC10GENICpossibly homozygous56554585
5154573792154573795GTT---30GENICheterozygous56554586
5154575571154575572C-10GENICheterozygous56532944
5154577319154577320CA11GENIChomozygous55803598
5154577321154577322CA11GENIChomozygous55803599
5154516616154516617CCTTTTTTTT8GENICheterozygous56461818
5154533145154533146A-4GENICheterozygous56461819
5154563620154563622GT--10GENICheterozygous56461821