chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144473794144473796AT33GENIChomozygous137347694
5144473962144473963CT41GENIChomozygous143966421
5144474333144474334GT12GENIChomozygous143966422
5144474359144474360CT11GENICpossibly homozygous143966423
5144475366144475367TC25GENIChomozygous143966424
5144475558144475558A39GENIChomozygous137347697
5144477199144477200GT34GENIChomozygous143966425
5144477245144477246TC34GENIChomozygous143966426
5144477535144477536GA44GENIChomozygous143966427
5144475484144475485TC25GENIChomozygous137645756
5144474329144474330G12GENICheterozygous137347695
5144474329144474330GT12GENIChomozygous403161875
5144482651144482652TG19GENIChomozygous143966428
5144482669144482670AG15GENIChomozygous137645761
5144482847144482847TC32GENIChomozygous137347698
5144483059144483060GA32GENIChomozygous137645762
5144485452144485453GA27GENIChomozygous143966429
5144486868144486869TC61GENIChomozygous137645767
5144487839144487840AG39GENIChomozygous143966430
5144487885144487886AG49GENIChomozygous143966431
5144487971144487972TC49GENIChomozygous143966432
5144489252144489253GA40GENIChomozygous143966433