chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172368440172368441AC69GENIChomozygous114092298
5172370066172370067TC59GENIChomozygous114092300
5172372561172372562TC51GENIChomozygous114092302
5172374917172374918GA79GENIChomozygous114092304
5172376738172376739TC53GENIChomozygous114092306
5172376821172376821AG50GENIChomozygous128276524
5172377725172377726GA75GENICpossibly homozygous114092308
5172377951172377952AC64GENIChomozygous114092310
5172378233172378234TC53GENIChomozygous114092312
5172378241172378241TTT55GENIChomozygous128276525
5172378284172378285TC53GENIChomozygous114092314
5172378708172378709CT46GENIChomozygous114092316
5172379585172379586GA68GENIChomozygous114092318
5172383433172383434TC41GENIChomozygous114092320
5172384071172384072CA57GENIChomozygous114092322
5172384072172384073TA57GENIChomozygous114092324