chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142900875142900876CT17GENIChomozygous56318789
7142902658142902659AG19GENIChomozygous56318793
7142902718142902719TA10GENICheterozygous56318795
7142902888142902889TG11GENIChomozygous54162001
7142902892142902893TC11GENIChomozygous54162002
7142902912142902913CG12GENIChomozygous54162003
7142903045142903046GT15GENIChomozygous54162005
7142903095142903096GA32GENICpossibly homozygous56318797
7142904803142904804CT13GENICpossibly homozygous56318799
7142904833142904834AT10GENIChomozygous56318801
7142905212142905213GT11GENIChomozygous56318803
7142905433142905434GA16GENICpossibly homozygous56318805
7142905568142905569TA16GENICpossibly homozygous56318807
7142906376142906377TA26GENICpossibly homozygous56318809
7142906400142906401GGA13GENICheterozygous56318811
7142906516142906517CT18GENIChomozygous56318813
7142906866142906867AG24GENICpossibly homozygous54162012
7142909886142909887CT14GENIChomozygous56318818
7142910246142910252TTTCCG------2GENIChomozygous56318821
7142911046142911047T-2GENIChomozygous54162022
7142913287142913288GT17GENICpossibly homozygous54162039
7142913707142913708CT12GENIChomozygous56318829
7142914055142914056GA14GENICpossibly homozygous56318831
7142914094142914095TTAG12GENIChomozygous54162040
7142914418142914419CT17GENICpossibly homozygous56318834
7142915480142915481GA17GENICpossibly homozygous54162044
7142916076142916077AG9GENIChomozygous54803005
7142918123142918124G-12GENICpossibly homozygous55883163
7142916911142916912AG21GENIChomozygous55883159
7142917456142917457AT16GENICpossibly homozygous55883161