chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113078059930780611GTTTCCGACTGG56GENIChomozygous146230957
113078064030780641G50GENIChomozygous138880798
113078168830781689CG55GENIChomozygous138952982
113078233230782333AC63GENIChomozygous138952984
113078396630783966CT41GENIChomozygous138880799
113078462730784628AG49GENIChomozygous138952987
113078278730782788AG52GENIChomozygous138952985
113078384430783845AG67GENIChomozygous138952986
113078172430781725TC45GENIChomozygous142282736
113078255330782554GA49GENIChomozygous146237195
113078478630784787C55GENIChomozygous138880800
113078602530786026TC55GENIChomozygous138952988
113078610730786108CG62GENIChomozygous138952989
113078663930786640AG62GENIChomozygous138952990
113078673030786731CG62GENIChomozygous138952991
113078690330786904CT47GENIChomozygous142282742
113078697330786974AG59GENIChomozygous138952992
113078766830787669G57GENIChomozygous138880801
113078800730788008TC47GENIChomozygous138952993
113078819130788192CT66GENIChomozygous138952994
113078831030788311TC76GENIChomozygous138952995
113078896430788965CA59GENIChomozygous146237196
113078921330789214CT47GENIChomozygous146237197
113078942130789422GA65GENIChomozygous142282745
113079062530790629CACA51GENIChomozygous138880802
113079084530790846AG51GENIChomozygous138952997
113079111430791115CA39GENIChomozygous138952998
113079172430791725GA51GENIChomozygous138952999
113079209130792092TA51GENIChomozygous138953000
113079241530792416T44GENICpossibly homozygous138880803
113079259530792596TA50GENIChomozygous138953002
113079310530793106G58GENIChomozygous146230958
113079367730793678CT42GENIChomozygous138953006
113079548830795489GA57GENIChomozygous138953008
113079626630796267TC44GENIChomozygous146237198
113079769530797696AG61GENIChomozygous138953013
113078554430785544G47GENIChomozygous142270291