chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105908500059085001AG24GENIChomozygous51464960
105908525459085255CT26GENIChomozygous51464961
105908745659087457TC18GENIChomozygous51464962
105908813359088134AG26GENIChomozygous51464963
105908994859089949A-20GENIChomozygous51464964
105909011959090120TTCA24GENIChomozygous51464965
105909012059090121GT24GENIChomozygous52319538
105909012259090123TTTTCAAAA23GENIChomozygous51464966
105909012459090125CA23GENIChomozygous52248798
105909027659090277CCT5GENICheterozygous52460809
105909162659091627CT24GENIChomozygous51464967
105909182459091825AAAAAACAAAAC22GENIChomozygous51464968
105909271859092719TTTGGA10GENIChomozygous51464969
105909311659093117AG26GENIChomozygous51464970
105909403959094040AG49GENIChomozygous51464971
105909416359094164TTA20GENIChomozygous51464972
105909480259094804CT--54GENIChomozygous51464973
105909487359094874GA29GENIChomozygous51464974
105909509159095092CT30GENIChomozygous51464975
105909509259095093AG31GENIChomozygous51464976
105909607559096076CCAAAAAAA2GENIChomozygous52378903
105909611059096111GA16GENIChomozygous51464977
105909665259096653TTC25GENIChomozygous51464978
105909675659096757CT34GENIChomozygous51464979
105909718559097186CT36GENIChomozygous51464980
105909816059098161TC28GENIChomozygous51464981
105909870459098705TA19GENIChomozygous51464982