chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108743106287431063GA17GENIChomozygous116899815
108743114287431143AC29GENICpossibly homozygous116899817
108743174487431745TC8GENICheterozygous116899821
108743205687432057CT18GENIChomozygous116899823
108743207887432079AG22GENIChomozygous116899825
108743230687432307CT22GENIChomozygous116899827
108743260687432607CT26GENIChomozygous116899829
108743350987433510AT22GENIChomozygous116899831
108743372387433724AG16GENIChomozygous116899833
108743384387433844AG22GENIChomozygous116899835
108743173387431734TG10GENICheterozygous118047595
108743396287433963CA22GENIChomozygous116899837
108743399087433991CG25GENIChomozygous116899839
108743639487436395TC12GENIChomozygous116899841
108743728887437289GT10GENIChomozygous116899843
108743741787437418CT25GENIChomozygous116899845