chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6111456744111456745GA32GENIChomozygous115154469
6111457253111457254TC9GENIChomozygous115154471
6111457438111457439TC4GENIChomozygous115154473
6111458247111458248CT12GENIChomozygous115154475
6111458442111458443AG33GENIChomozygous115154481
6111459831111459832AG40GENIChomozygous115154483
6111459880111459881TG24GENICheterozygous118733299
6111460379111460380AC21GENIChomozygous115154489
6111467789111467790GA20GENIChomozygous115154499
6111467984111467985CT27GENIChomozygous115154501
6111469351111469352GC21GENIChomozygous115154503
6111469713111469714TC16GENIChomozygous115154505
6111469964111469965CA37GENIChomozygous115154507
6111470006111470007CA35GENIChomozygous115154509
6111470208111470209AG16GENIChomozygous115154511
6111471583111471584TC25GENIChomozygous115154513
6111471836111471837TC23GENIChomozygous115154515
6111472160111472161AG18GENIChomozygous115154517
6111472804111472805TC30GENIChomozygous115154519
6111472883111472884CA27GENIChomozygous115154521
6111473124111473125AT17GENIChomozygous115154523
6111473143111473144TC9GENIChomozygous115154525
6111474349111474350GT17GENIChomozygous115154533
6111474927111474928TC15GENIChomozygous115154535
6111476025111476026CG23GENIChomozygous115154537
6111476038111476039AT21GENIChomozygous115154539
6111476131111476132CT14GENIChomozygous115154541
6111476608111476609CT10GENIChomozygous115154543