chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105908500059085001AG30GENIChomozygous51464960
105908745659087457TC20GENIChomozygous51464962
105908813359088134AG29GENIChomozygous51464963
105909011959090120TTCA26GENIChomozygous51464965
105909012059090121GT26GENIChomozygous52319538
105909012259090123TTTTCAAAA25GENIChomozygous51464966
105909012459090125CA23GENIChomozygous52248798
105909025759090259TT--13GENIChomozygous52062021
105909027659090277CCT8GENICheterozygous52460809
105909091559090916CT31GENIChomozygous52062023
105909125359091254CT16GENIChomozygous52062025
105909162659091627CT28GENIChomozygous51464967
105909182459091825AAAAAACAAAAC25GENIChomozygous51464968
105909271959092743TGGATGGATGGATGGATGGATGGA------------------------13GENIChomozygous52319540
105909294059092941AG23GENIChomozygous52062029
105909311659093117AG18GENIChomozygous51464970
105909403959094040AG25GENIChomozygous51464971
105909416359094164TTA22GENIChomozygous51464972
105909480259094804CT--22GENIChomozygous51464973
105909487359094874GA15GENIChomozygous51464974
105909509159095092CT25GENIChomozygous51464975
105909509259095093AG25GENIChomozygous51464976
105909559759095598CT15GENIChomozygous52062031
105909611059096111GA18GENIChomozygous51464977
105909623359096234CT21GENIChomozygous52062033
105909740859097409TC19GENIChomozygous52062035
105909903459099040GGCGGC------19GENIChomozygous52460810
105909607559096076CCAAAAAAA12GENIChomozygous52378903