chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34260590642605907GA30GENIChomozygous58416903
34260608842606089CT15GENIChomozygous58122671
34260627842606282TTTG----12GENICheterozygous58122673
34260627942606282TTG---10GENIChomozygous58122674
34260631942606320AG18GENIChomozygous58416904
34260669342606694GC20GENICheterozygous58122677
34260669342606694GGTC16GENICpossibly homozygous58122678
34260758642607587C-24GENIChomozygous58416905
34260766342607664CT29GENIChomozygous58416906
34260770442607705GA34GENIChomozygous58416907
34260787242607873GGA25GENIChomozygous58122680
34260795642607957AG28GENICpossibly homozygous58122682
34260838942608390T-26GENICheterozygous58122692
34260860942608610GC29GENIChomozygous58416908
34260870442608705TA23GENIChomozygous58122696
34260883442608838GTGT----4GENIChomozygous58416909
34260979742609798CT14GENIChomozygous58416910
34261003442610035CT30GENIChomozygous58416911
34261009542610096GA23GENIChomozygous58122698
34261040342610404TA16GENIChomozygous58416912
34261055542610556GC29GENIChomozygous58122701
34261059142610592AG30GENIChomozygous58122702
34261073542610736CA24GENIChomozygous58122703
34261075842610759AG19GENIChomozygous58122704
34261095542610956AG31GENIChomozygous58122706
34261096042610961TC29GENIChomozygous58122707
34261097542610976CA24GENIChomozygous58349174
34261128842611289AG38GENIChomozygous58416913
34261183042611832GA--2GENIChomozygous57346233
34261183742611838C-2GENIChomozygous57346235
34261184242611845GCC---2GENIChomozygous57346237
34261185042611851G-2GENIChomozygous57346239
34261187042611872CG--1GENIChomozygous57346243
34261187542611876G-7GENICpossibly homozygous57346245
34261188242611883C-9GENIChomozygous57346247
34261199442611995CT20GENIChomozygous58122718
34261224342612244GA23GENIChomozygous58416914
34261233342612334GA27GENIChomozygous58349186
34261257042612571AG32GENIChomozygous58122723
34261257142612572GC33GENIChomozygous58122724
34261259142612592AG30GENIChomozygous58122725
34261269042612691TC26GENIChomozygous58122726