chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113078059930780611GTTTCCGACTGG66GENIChomozygous146230957
113078064030780641G58GENIChomozygous138880798
113078168830781689CG55GENIChomozygous138952982
113078233230782333AC59GENIChomozygous138952984
113078278730782788AG63GENIChomozygous138952985
113078172430781725TC56GENIChomozygous142282736
113078255330782554GA48GENIChomozygous146237195
113078384430783845AG62GENIChomozygous138952986
113078396630783966CT58GENIChomozygous138880799
113078462730784628AG52GENIChomozygous138952987
113078478630784787C47GENIChomozygous138880800
113078602530786026TC37GENIChomozygous138952988
113078610730786108CG45GENIChomozygous138952989
113078663930786640AG51GENIChomozygous138952990
113078673030786731CG50GENIChomozygous138952991
113078690330786904CT44GENIChomozygous142282742
113078697330786974AG48GENIChomozygous138952992
113078766830787669G58GENIChomozygous138880801
113078800730788008TC60GENIChomozygous138952993
113078819130788192CT63GENIChomozygous138952994
113078831030788311TC53GENIChomozygous138952995
113078896430788965CA46GENIChomozygous146237196
113078921330789214CT54GENIChomozygous146237197
113078942130789422GA44GENIChomozygous142282745
113079062530790629CACA56GENIChomozygous138880802
113079084530790846AG57GENIChomozygous138952997
113079111430791115CA30GENIChomozygous138952998
113079172430791725GA41GENIChomozygous138952999
113079209130792092TA52GENIChomozygous138953000
113079241530792416T45GENICpossibly homozygous138880803
113079259530792596TA61GENIChomozygous138953002
113079310530793106G46GENICpossibly homozygous146230958
113079367730793678CT52GENIChomozygous138953006
113079548830795489GA62GENIChomozygous138953008
113079626630796267TC53GENIChomozygous146237198
113079769530797696AG47GENIChomozygous138953013
113078554430785544G54GENIChomozygous142270291
113079109930791100GA34GENICheterozygous154691226
113079109930791100G34GENIChomozygous403302807