chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6111456744111456745GA25GENIChomozygous115154469
6111457253111457254TC18GENIChomozygous115154471
6111457438111457439TC16GENIChomozygous115154473
6111458247111458248CT16GENIChomozygous115154475
6111458442111458443AG24GENIChomozygous115154481
6111459831111459832AG40GENIChomozygous115154483
6111460336111460337TC30GENIChomozygous115154485
6111460337111460338GA30GENIChomozygous115154487
6111460379111460380AC31GENIChomozygous115154489
6111467789111467790GA18GENIChomozygous115154499
6111467984111467985CT21GENIChomozygous115154501
6111469351111469352GC14GENIChomozygous115154503
6111469713111469714TC25GENIChomozygous115154505
6111469964111469965CA27GENIChomozygous115154507
6111470006111470007CA30GENICpossibly homozygous115154509
6111470208111470209AG29GENIChomozygous115154511
6111471583111471584TC23GENIChomozygous115154513
6111471836111471837TC32GENIChomozygous115154515
6111472160111472161AG14GENICpossibly homozygous115154517
6111472804111472805TC19GENIChomozygous115154519
6111472883111472884CA21GENIChomozygous115154521
6111473124111473125AT22GENIChomozygous115154523
6111473143111473144TC20GENIChomozygous115154525
6111473289111473290CT12GENIChomozygous115154527
6111474349111474350GT21GENIChomozygous115154533
6111474927111474928TC28GENIChomozygous115154535
6111476025111476026CG16GENIChomozygous115154537
6111476038111476039AT17GENIChomozygous115154539
6111476131111476132CT27GENIChomozygous115154541
6111476608111476609CT8GENIChomozygous115154543
6111476656111476657TC10GENIChomozygous115154545