chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134985338049853381GT22GENICpossibly homozygous114338656
134985458149854581AAGGAAGAAA9GENIChomozygous129052398
134985482949854829T15GENIChomozygous129052409
134985483749854837G17GENIChomozygous129052410
134985485049854850TG17GENIChomozygous129052411
134985487349854873A18GENIChomozygous129052412
134985488049854881G18GENIChomozygous129052413
134985488849854889TC18GENIChomozygous114338658
134985488949854890CT18GENIChomozygous115198834
134986109549861096AG8GENIChomozygous114967710
134986109949861100AG8GENIChomozygous114967712
134986110449861105CG6GENIChomozygous114967714
134986110549861106CG5GENIChomozygous114967716
134986109849861099CA8GENIChomozygous114720279
134986478349864783TC22GENIChomozygous129052421
134986501249865012CGTATGCACACC10GENIChomozygous129052422
134989803949898040G20GENIChomozygous129052440
134989804349898043C22GENIChomozygous129052441
134989808949898090A19GENIChomozygous129052442
134989816049898162GT20GENIChomozygous129052443
134989829349898293G20GENIChomozygous129052444
134989831649898316T19GENIChomozygous129052445
134989850449898504A5GENIChomozygous129052446
134989852549898526G5GENIChomozygous129052447
134989853149898532G5GENIChomozygous129052448
134989856349898564T8GENIChomozygous129052449
134989859549898595C10GENIChomozygous129052450
134989860649898607CT12GENIChomozygous114338848
134989860749898608AC12GENIChomozygous123732074
134989861649898617C14GENIChomozygous129052451