chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1294222729422273AG30GENIChomozygous143527375
1294228209422821CG14GENIChomozygous145773099
1294229599422960GC14GENIChomozygous143527376
1294233229423323GA15GENICheterozygous403315492
1294233229423323G15GENIChomozygous403315493
1294234339423434TC16GENIChomozygous139079866
1294243309424331CT22GENIChomozygous145773100
1294243709424371CT21GENIChomozygous145773101
1294244349424435AG20GENIChomozygous143527378
1294244629424463GT16GENICheterozygous154752474
1294244629424463G16GENICpossibly homozygous403315494
1294247509424751TC17GENIChomozygous139079870
1294255359425536TC20GENIChomozygous139079871
1294256659425666CT24GENIChomozygous145773102
1294256779425678AG22GENIChomozygous139079872
1294256929425693AG20GENIChomozygous139079873
1294266659426666GA31GENIChomozygous139079875
1294244469424446GG20GENIChomozygous145770432
1294244609424463TTG16GENICpossibly homozygous145770433
1294268859426886G10GENICheterozygous403315495
1294268859426886GA10GENIChomozygous403315496
1294269479426948TC18GENIChomozygous139079877
1294278679427868GA30GENIChomozygous139079878
1294280329428033TC29GENIChomozygous139079879
1294280499428050TC32GENIChomozygous139079880