chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1294217609421761TC13GENIChomozygous139079859
1294219299421930TA25GENIChomozygous139079860
1294221579422158AG24GENIChomozygous139079861
1294221869422187GA21GENIChomozygous139079862
1294233139423314TA4GENIChomozygous139079863
1294233149423315TA4GENIChomozygous139079864
1294234319423432CT17GENIChomozygous139079865
1294234339423434TC17GENIChomozygous139079866
1294240019424002AT29GENIChomozygous139079867
1294241189424119AG31GENIChomozygous139079868
1294242029424203AG24GENICpossibly homozygous139079869
1294247509424751TC10GENIChomozygous139079870
1294255359425536TC18GENIChomozygous139079871
1294256779425678AG19GENIChomozygous139079872
1294256929425693AG22GENIChomozygous139079873
1294259689425969TA25GENIChomozygous139079874
1294266659426666GA27GENIChomozygous139079875
1294267599426760TG24GENIChomozygous139079876
1294268859426886G9GENICheterozygous403315495
1294268859426886GA9GENICheterozygous403315496
1294269479426948TC16GENIChomozygous139079877
1294278679427868GA14GENIChomozygous139079878
1294280329428033TC18GENIChomozygous139079879
1294280499428050TC20GENIChomozygous139079880
1294236949423704GCGTGCGTGC16GENIChomozygous139039799
1294234059423406A14GENIChomozygous139039797
1294236909423692GC16GENIChomozygous139039798