chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105758343457583435GC47GENIChomozygous116603949
105758413957584140AT61GENIChomozygous116603951
105758474257584743A59GENIChomozygous128819800
105758709957587100AG53GENIChomozygous116603953
105758793357587934TC50GENIChomozygous116603955
105758815957588160CT60GENIChomozygous116603957
105758837057588371A53GENIChomozygous128819801
105758854957588550TC46GENIChomozygous116603959
105758859857588601AAC40GENIChomozygous128819802
105758864057588641GA46GENIChomozygous116603961
105758871257588713TC66GENIChomozygous116603963
105759078157590782GA59GENIChomozygous116603965
105759089757590898AG41GENIChomozygous116603967
105759125657591257AT67GENIChomozygous116603969
105759133557591336TC56GENIChomozygous116603971
105759153657591537AT56GENIChomozygous116603973
105759289157592892GA68GENIChomozygous116603975
105759539557595396AG36GENIChomozygous116603977
105759578257595783AG54GENIChomozygous116603979
105759594557595946AG47GENIChomozygous116603981
105759617757596178AG46GENIChomozygous116603983
105759627257596273AG49GENIChomozygous116603985
105759649757596515ATACATATACATACATAC1GENIChomozygous128819803
105759752857597529TC53GENIChomozygous116603989
105759765457597655GA51GENIChomozygous116603991
105759823357598234TC55GENIChomozygous116603993
105759867157598672CT73GENIChomozygous116603995
105759881757598818AT57GENIChomozygous116603997
105759955557599556CT56GENIChomozygous116603999
105759963657599636T65GENIChomozygous128819805
105760132357601323GATGTGTGAGGCAGGAAGGCAGAGGCAGGTG47GENIChomozygous128819806
105760181057601811GC56GENIChomozygous116604001
105760336657603367AC75GENIChomozygous116604003
105760382057603821TA68GENIChomozygous116604005
105760404957604050CA57GENIChomozygous116604007
105760405057604051AG57GENIChomozygous116604009
105760443357604434CG59GENIChomozygous116890323
105760479657604797CT46GENIChomozygous116604011
105760489257604892GG48GENIChomozygous128819807
105759658057596581TC12GENIChomozygous128869701
105759737857597379AG12GENIChomozygous128869702