chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138438507784385078AC66GENICpossibly homozygous142406527
138438508084385081AG64GENIChomozygous142406528
138438524384385244AG53GENIChomozygous149415561
138438859584388596AG66GENIChomozygous142406533
138438925884389260TA45GENIChomozygous142351682
138439024684390247CT42GENIChomozygous149415562
138439131084391311CT58GENIChomozygous149415563
138439207784392078GA70GENIChomozygous149415564
138439328484393285AC71GENIChomozygous142406561
138439483584394836TC60GENIChomozygous142406567
138438754784387559AGGAAGGAAGGA54GENIChomozygous149398806
138439033884390338TCC26GENICheterozygous149398807
138439453784394537GG30GENIChomozygous149398808
138439522084395221CT36GENICpossibly homozygous149415565
138439567484395675AG68GENIChomozygous142406569
138439579284395793AT67GENIChomozygous149415566
138439617784396178GT62GENIChomozygous142406573
138439581784395818TC69GENIChomozygous149415567
138439589884395899CT52GENIChomozygous149415568
138439616584396166GA61GENIChomozygous142406572
138439625284396253AG72GENIChomozygous142406574
138439642084396421GA59GENIChomozygous149415569
138439691284396913TA60GENIChomozygous149415570
138439715384397154TC62GENIChomozygous149415571
138439727784397277C59GENIChomozygous149398809
138439727884397279AC61GENIChomozygous149415572
138439730584397306AG69GENIChomozygous149415573
138439734284397343TG72GENICpossibly homozygous149415574
138439747884397479AG55GENIChomozygous149415575
138439836184398362CA15GENIChomozygous142406577
138440066884400669TA82GENIChomozygous142406579
138440098484400985GA74GENIChomozygous149415576
138440146484401465G59GENIChomozygous149398810
138440146684401469CGG60GENIChomozygous149398811
138440168184401682GA44GENIChomozygous149415577
138440180484401805GA54GENIChomozygous149415578
138440192784401936TCAACGTCG63GENIChomozygous149398812
138440392984403930CT61GENIChomozygous149415579
138440488984404890TC55GENIChomozygous142406581