chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG6GENIChomozygous931976757
4140887405140887406GC10GENIChomozygous931976758
4140887526140887527AG10GENIChomozygous931976759
4140892114140892115TA10GENIChomozygous931976760
4140894149140894150GA14GENIChomozygous931976761
4140894483140894484TC9GENIChomozygous931976762
4140894658140894659GC10GENIChomozygous931976763
4140896988140896989GA4GENIChomozygous931976764
4140899328140899329GA5GENIChomozygous931976765
4140901019140901020TC10GENIChomozygous931976766
4140902715140902716TC15GENIChomozygous931976767
4140902957140902958AG8GENIChomozygous931976768
4140903807140903808CT10GENIChomozygous931976769
4140906395140906396AG5GENIChomozygous931976770
4140907775140907776TG5GENIChomozygous931976771
4140908274140908275TG10GENIChomozygous931976772
4140908994140908995GC11GENIChomozygous931976773
4140909042140909043GA12GENIChomozygous931976774
4140909059140909060CA13GENIChomozygous931976775
4140909109140909110GA6GENIChomozygous931976776
4140909129140909130CT6GENIChomozygous931976777
4140909170140909171GA10GENIChomozygous931976778
4140909196140909197CT13GENIChomozygous931976779
4140909244140909245GT16GENIChomozygous931976780
4140909248140909249TA16GENIChomozygous931976781
4140909269140909270GA13GENIChomozygous931976782
4140909286140909287GC13GENIChomozygous931976783
4140916630140916631TG5GENIChomozygous931976784
4140916631140916632CA5GENIChomozygous931976785
4140916937140916938GA3GENIChomozygous931976786