chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37884574978845762ATGTCTGAACAGT-------------27GENIChomozygous58157865
37884599178845992AT30GENIChomozygous58157869
37884608778846088CCAG34GENIChomozygous58597976
37884626378846264CT42GENIChomozygous57479250
37884630378846304AG25GENIChomozygous57479251
37884638078846381AT33GENIChomozygous58157871
37884669178846692CT31GENIChomozygous58157873
37884669778846698AG32GENIChomozygous58157875
37884760878847612ATAT----14GENIChomozygous58157877
37884923578849236TC22GENIChomozygous58157879
37885013778850138TA25GENIChomozygous57479272
37885072878850729TC30GENIChomozygous57479278
37885074778850748AAAC16GENICpossibly homozygous58157883
37885111578851116AACG36GENIChomozygous58157885
37885434778854348GGGT17GENICheterozygous57479315
37885434778854348GGGTGT17GENICpossibly homozygous57479317
37885515778855158T-25GENIChomozygous57479331
37885516778855168TA29GENIChomozygous58551585
37885568678855687T-11GENICheterozygous58668065
37885751878857519CCA17GENIChomozygous58157887
37885812078858121CCTT12GENIChomozygous57479349
37885874878858749GGAGCAGCAGC11GENICpossibly homozygous58597978
37885874878858749GGAGCAGC11GENICheterozygous58649888
37885883378858834AG43GENIChomozygous57479355
37885936678859367CT33GENIChomozygous58157889
37886098278860983TG20GENIChomozygous58157891
37886098778860988AG20GENIChomozygous58157893
37886163378861634CT44GENIChomozygous58157895
37886217878862179GT19GENIChomozygous57479377
37886223178862232TA21GENIChomozygous57479379
37886465878864659CT21GENIChomozygous58157897
37886468678864731CACACACACACACACACACACACACACACACACACACACACACAC---------------------------------------------11GENICpossibly homozygous58597980
37886502478865025TC35GENIChomozygous57479389
37886552778865539CAGCAGCAGCAG------------21GENIChomozygous58157899