chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105880675158806751AAGAA74GENICpossibly homozygous131095127
105880693758806938GA47GENIChomozygous116937144
105880704158807042AT65GENIChomozygous116937146
105880733358807334AG81GENIChomozygous116937152
105880772258807723TC53GENIChomozygous116937158
105880863658808637CA53GENIChomozygous117079400
105880901458809015GC71GENIChomozygous116937164
105880928458809285AT60GENIChomozygous117079401
105881067658810677AT70GENIChomozygous117079403
105881092058810921GC58GENIChomozygous116937170
105881115958811160TC65GENIChomozygous116937172
105881132458811325AG64GENIChomozygous116937174
105881174158811742CT46GENIChomozygous117079404
105881174158811741G45GENIChomozygous131095128
105881176358811764GA50GENIChomozygous117079406
105881269058812691AC67GENICpossibly homozygous116937176
105881376958813770GT53GENICpossibly homozygous116937182
105881399158813992GA64GENIChomozygous116937184
105881086558810866CT63GENIChomozygous116607204
105881364358813644AG46GENIChomozygous116607206
105881368858813689CT47GENIChomozygous116607208