chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148193220281932203CT10GENIChomozygous144135916
148193236681932367CT18GENIChomozygous144135917
148193238381932384GC20GENIChomozygous144135918
148193249781932498GA13GENICpossibly homozygous147050934
148193251781932527GTGTGTGAGA11GENIChomozygous147043461
148193256781932568TC10GENIChomozygous147050935
148193258481932584AGAGAC8GENIChomozygous147043462
148193270181932702A7GENIChomozygous144107314
148193256781932568T10GENICheterozygous403852701
148193270681932707A7GENIChomozygous144107315
148195567281955673GA19GENICpossibly homozygous403364202
148195567281955673G19GENICheterozygous403364203
148201357282013573CT20GENIChomozygous139576611
148201359082013590ATCGTGTACACCAGC18GENIChomozygous139406710
148201417482014175CT16GENIChomozygous139576612
148201520482015205GA26GENIChomozygous139576613
148201544982015450GA20GENIChomozygous139576614
148201584782015848TC28GENIChomozygous139576615
148201804282018043CT16GENIChomozygous139576616
148201811882018119TC20GENIChomozygous139576617
148201846882018469AG23GENIChomozygous139576618
148201882582018826GA23GENIChomozygous139576619
148201979982019800TC18GENIChomozygous139576620