chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2219071796219071797GA19GENIChomozygous110823594
2219072481219072482GA32GENIChomozygous110823595
2219074192219074193AG18GENIChomozygous110247849
2219076035219076036CT24GENIChomozygous110247851
2219076069219076070GA29GENIChomozygous110247853
2219077061219077062AC10GENIChomozygous110247855
2219077440219077441TC15GENIChomozygous110247859
2219077942219077943AC21GENIChomozygous110247861
2219079059219079060TA21GENIChomozygous110823596
2219079224219079225CT24GENIChomozygous110247863
2219079230219079231CT25GENIChomozygous110247865
2219079842219079843AG18GENIChomozygous110247867
2219079933219079934AG33GENIChomozygous110247869
2219080032219080033TC20GENIChomozygous110247871
2219080181219080182CA16GENIChomozygous110247873
2219080465219080466CT28GENIChomozygous110247877
2219080549219080550CT32GENIChomozygous110247879
2219080946219080947TC21GENIChomozygous110247881
2219081071219081072TC13GENIChomozygous110247883
2219081227219081228TA16GENIChomozygous110247887
2219081254219081255GT23GENIChomozygous110247889
2219081272219081273CG21GENIChomozygous110247891
2219081280219081281CT22GENIChomozygous110247893
2219081288219081289CT19GENIChomozygous110247895
2219081380219081381AT21GENIChomozygous110247897
2219081411219081412CG21GENIChomozygous110247899
2219081432219081433CT19GENIChomozygous110247901
2219081461219081462GA19GENIChomozygous110247903
2219081533219081534AG22GENIChomozygous110247905
2219082790219082791CT23GENIChomozygous110247910
2219082866219082867TC29GENIChomozygous110247912
2219083303219083304GT27GENIChomozygous110247914
2219084054219084055TG21GENIChomozygous110247916
2219084580219084581AG19GENIChomozygous110247918
2219084607219084608CT18GENICpossibly homozygous110247920