chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109038326990383270C58GENIChomozygous128844154
109038329590383296AT48GENICpossibly homozygous116676190
109038329890383300CT48GENICpossibly homozygous128844155
109038333990383340T57GENIChomozygous128844156
109038357590383576TA30GENIChomozygous116676192
109038465690384657GC47GENICpossibly homozygous116676194
109038492090384921GA58GENICpossibly homozygous116676196
109038556490385565TC66GENIChomozygous116676198
109038557290385573G65GENIChomozygous128844157
109038572790385728A65GENIChomozygous128844158
109038671690386717AC76GENIChomozygous116676200
109038966390389664CT75GENIChomozygous116676202
109039038390390384GA60GENIChomozygous116676204
109039123090391231GA76GENIChomozygous116676206
109039220590392206CT49GENIChomozygous116676208