chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134985338049853381GT20GENICpossibly homozygous114338656
134985458149854581AAGGAAGAAA31GENIChomozygous129052398
134985464049854641T21GENIChomozygous129052399
134985464849854649A19GENIChomozygous129052400
134985466349854664G18GENIChomozygous129052402
134985467349854674A19GENIChomozygous129052403
134985469049854692TC17GENIChomozygous129052404
134985470049854701A13GENIChomozygous129052405
134985474449854747TGT1GENIChomozygous132341362
134985478349854783A1GENIChomozygous129052407
134985478749854787T1GENIChomozygous129052408
134985482949854829T29GENIChomozygous129052409
134985483749854837G27GENIChomozygous129052410
134985485049854850TG25GENIChomozygous129052411
134985487349854873A24GENIChomozygous129052412
134985488049854881G27GENIChomozygous129052413
134985488849854889TC26GENIChomozygous114338658
134985488949854890CT25GENIChomozygous115198834
134986109549861096AG11GENIChomozygous114967710
134986113149861132TG11GENIChomozygous118535401
134986116749861168AG4GENIChomozygous115024888
134986110549861106CG10GENIChomozygous114967716
134986109849861099CA10GENIChomozygous114720279
134986478349864783TC15GENIChomozygous129052421
134986501249865012CGTATGCACACC22GENIChomozygous129052422
134989803949898040G25GENIChomozygous129052440
134986109949861100AG10GENIChomozygous114967712
134986110449861105CG10GENIChomozygous114967714
134989804349898043C25GENIChomozygous129052441
134989808949898090A23GENIChomozygous129052442
134989816049898162GT24GENIChomozygous129052443
134989829349898293G25GENIChomozygous129052444
134989831649898316T23GENIChomozygous129052445
134989850449898504A5GENIChomozygous129052446
134989852549898526G6GENIChomozygous129052447
134989853149898532G6GENIChomozygous129052448
134989856349898564T9GENIChomozygous129052449
134989859549898595C13GENIChomozygous129052450
134989860649898607CT13GENIChomozygous114338848
134989860749898608AC13GENIChomozygous123732074
134989861649898617C13GENIChomozygous129052451