chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36348047563480476AAGCGC13GENIChomozygous57403823
36348048163480482CCGCGCG8GENICpossibly homozygous57403824
36348048163480482CCGCG8GENICheterozygous57892419
36348250163482502TC23GENIChomozygous57403830
36348350963483510TC25GENIChomozygous57403836
36348785563487856CCA5GENIChomozygous57403846
36349069363490694AG28GENIChomozygous57403854
36349126263491263GA22GENIChomozygous57403855
36349475663494757TC27GENIChomozygous57403861
36349881663498821TTTTT-----5GENIChomozygous57892427
36350219263502195AAA---1GENIChomozygous57403880
36350374163503742AG12GENICheterozygous58291595
36350375663503757GA13GENICpossibly homozygous58150462
36350377363503774GA17GENICheterozygous58150464
36350381363503814AG13GENICheterozygous58291597
36350628863506290GT--27GENIChomozygous57403904
36350731963507320AATT13GENIChomozygous58150468
36350734263507343C-12GENIChomozygous58150470
36350763063507631TC31GENIChomozygous57403908
36350765163507652CT31GENIChomozygous58150472
36350780763507808GA26GENIChomozygous57403909
36350813063508131GT18GENIChomozygous58150474
36350998163509986GATTA-----24GENICheterozygous58150476
36351017263510173CT23GENIChomozygous57403918
36351189763511898CCT32GENICheterozygous57403921
36351190263511903CCA30GENICheterozygous57403922
36351190463511905CCT28GENICheterozygous57403923
36351295363512955TG--21GENICheterozygous57892440
36351556863515569TC16GENIChomozygous58150478
36351730263517303TG28GENIChomozygous57403930
36351797263517973TTA24GENIChomozygous57403931
36351864263518644CC--20GENICheterozygous57403932
36351864363518644C-20GENICpossibly homozygous57403933
36351882163518822GA11GENIChomozygous57403935
36351908563519086GA27GENIChomozygous57403936
36351913063519131TC24GENIChomozygous57403937