chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2219071796219071797GA17GENIChomozygous110823594
2219072481219072482GA50GENIChomozygous110823595
2219074192219074193AG28GENIChomozygous110247849
2219076035219076036CT33GENIChomozygous110247851
2219076069219076070GA32GENIChomozygous110247853
2219077061219077062AC32GENIChomozygous110247855
2219077440219077441TC39GENIChomozygous110247859
2219077942219077943AC55GENIChomozygous110247861
2219079059219079060TA6GENIChomozygous110823596
2219079224219079225CT18GENIChomozygous110247863
2219079230219079231CT19GENIChomozygous110247865
2219079842219079843AG19GENIChomozygous110247867
2219079933219079934AG31GENIChomozygous110247869
2219080032219080033TC16GENIChomozygous110247871
2219080181219080182CA4GENIChomozygous110247873
2219080465219080466CT26GENIChomozygous110247877
2219080549219080550CT29GENIChomozygous110247879
2219080946219080947TC35GENIChomozygous110247881
2219081071219081072TC18GENIChomozygous110247883
2219081175219081176GA3GENIChomozygous110247885
2219081227219081228TA2GENIChomozygous110247887
2219081272219081273CG7GENIChomozygous110247891
2219081280219081281CT8GENIChomozygous110247893
2219081288219081289CT8GENIChomozygous110247895
2219081380219081381AT20GENIChomozygous110247897
2219081411219081412CG15GENIChomozygous110247899
2219081432219081433CT11GENIChomozygous110247901
2219081461219081462GA12GENIChomozygous110247903
2219081533219081534AG26GENIChomozygous110247905
2219082790219082791CT31GENIChomozygous110247910
2219082866219082867TC35GENIChomozygous110247912
2219083303219083304GT28GENIChomozygous110247914
2219084054219084055TG16GENIChomozygous110247916