chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5127512299127512300TG11GENIChomozygous56892695
5127512350127512351TG6GENICheterozygous55701804
5127512854127512855CT18GENICpossibly homozygous56230475
5127512949127512950CG4GENIChomozygous56230476
5127513011127513012GA11GENIChomozygous56892697
5127513333127513334CA6GENICheterozygous56230478
5127513543127513544GA14GENIChomozygous56892699
5127513718127513719TC28GENICpossibly homozygous55701806
5127513719127513720GA28GENICpossibly homozygous56289661
5127513943127513944GA16GENICpossibly homozygous56892701
5127514746127514747GT23INTERGENICpossibly homozygous55701810
5127515765127515766TG24INTERGENICpossibly homozygous55701820
5127517683127517684AT7INTERGENIChomozygous55701834
5127517700127517701TC5INTERGENIChomozygous56892705
5127517926127517927TC1INTERGENIChomozygous55701850
5127517932127517933TTA1INTERGENIChomozygous55701852
5127517947127517948TA3INTERGENIChomozygous55701856
5127517948127517949AG3INTERGENIChomozygous55701858
5127518026127518027AG8INTERGENICpossibly homozygous55701860
5127519891127519892AG13INTERGENICpossibly homozygous55701864
5127519897127519898GT12INTERGENIChomozygous55701866
5127520361127520362GA1INTERGENIChomozygous55701870
5127521158127521159CT12INTERGENICpossibly homozygous55701876
5127521470127521471CCA3INTERGENIChomozygous55701878
5127521735127521736AG17INTERGENICpossibly homozygous55701880
5127522330127522331TC14INTERGENICpossibly homozygous55701882
5127522959127522960AT18INTERGENICpossibly homozygous56892707