chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178526948178526949CT35GENIChomozygous954044892
1178527101178527102AG20GENIChomozygous954044893
1178527840178527841TC21GENIChomozygous954044894
1178528043178528044TA13GENIChomozygous954044895
1178529589178529590GA22GENIChomozygous954044896
1178530100178530101GT21GENIChomozygous954044897
1178530738178530739CA29GENIChomozygous954044898
1178530884178530885AT24GENIChomozygous954044899
1178531607178531608GA22GENIChomozygous954044900
1178531673178531674AT27GENIChomozygous954044901
1178532437178532438GA10GENIChomozygous954044902
1178532438178532439AG10GENIChomozygous954044903