chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102590426725904268AG23GENIChomozygous116748284
102590515325905154AG30GENIChomozygous116748288
102590522425905225CG28GENIChomozygous116526667
102590591125905912AT3GENICheterozygous117055159
102590591325905914AT3GENICheterozygous117055161
102590602825906029TA26GENIChomozygous116748290
102590631925906320AG29GENIChomozygous116748292
102590653225906533GA22GENIChomozygous116526669
102590653525906536GA23GENIChomozygous116526671
102590655425906555TC24GENIChomozygous116864426
102590656025906561TC26GENIChomozygous116526673
102590656325906564TC27GENIChomozygous116526675
102590658125906582AC24GENIChomozygous116526677
102590659125906592CA24GENIChomozygous116526679
102590667725906678T22GENIChomozygous131090011
102590671525906716GA20GENIChomozygous116526681
102590674125906743AT20GENIChomozygous131090012
102590749325907494GA21GENIChomozygous116526683
102590657325906576GGG26GENIChomozygous128798797
102590927925909280CT31GENIChomozygous116748294
102590997725909978CT22GENIChomozygous116748296
102590657925906579CTG26GENIChomozygous128798798