chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37884574978845762ATGTCTGAACAGT-------------31GENIChomozygous58157865
37884599178845992AT29GENIChomozygous58157869
37884608778846088CCAG37GENIChomozygous58597976
37884626378846264CT27GENIChomozygous57479250
37884630378846304AG29GENIChomozygous57479251
37884638078846381AT20GENIChomozygous58157871
37884669178846692CT22GENIChomozygous58157873
37884669778846698AG23GENIChomozygous58157875
37884923578849236TC13GENIChomozygous58157879
37885013778850138TA27GENIChomozygous57479272
37885072878850729TC20GENIChomozygous57479278
37885074778850748AAAC17GENICpossibly homozygous58157883
37885111578851116AACG38GENIChomozygous58157885
37885434778854348GGGT11GENICheterozygous57479315
37885434778854348GGGTGT11GENICheterozygous57479317
37885515778855158T-13GENIChomozygous57479331
37885516778855168TA13GENIChomozygous58551585
37885751878857519CCA17GENIChomozygous58157887
37885812078858121CCTT9GENIChomozygous57479349
37885874878858749GGAGCAGCAGC8GENIChomozygous58597978
37885883378858834AG24GENIChomozygous57479355
37885936678859367CT28GENIChomozygous58157889
37886098278860983TG12GENIChomozygous58157891
37886098778860988AG13GENIChomozygous58157893
37886163378861634CT19GENIChomozygous58157895
37886217878862179GT20GENIChomozygous57479377
37886223178862232TA22GENICpossibly homozygous57479379
37886465878864659CT15GENIChomozygous58157897
37886468678864731CACACACACACACACACACACACACACACACACACACACACACAC---------------------------------------------8GENIChomozygous58597980
37886502478865025TC19GENIChomozygous57479389
37886552778865539CAGCAGCAGCAG------------13GENIChomozygous58157899