chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117900724479007245GA15GENICpossibly homozygous67422009
117901091179010912GA20GENIChomozygous67422011
117901487879014879GA13GENIChomozygous67422013
117901762879017629TC23GENIChomozygous67422015
117902047779020478CT23GENIChomozygous67084546
117902057579020576CT32GENICpossibly homozygous67422017
117900930879009309TA20GENICheterozygous67499777
117901374479013745CT29GENICheterozygous67499779
117901120679011207GC5GENIChomozygous68196869
117902241979022420TC15GENICpossibly homozygous67499780
117902335279023353TC16GENIChomozygous67422019
117902725579027256GA13GENICpossibly homozygous67422021
117902756779027568CG26GENICpossibly homozygous67422023
117902821879028219CT30GENICpossibly homozygous67084551
117902845979028460TC20GENIChomozygous67084553
117902896279028963CA18GENIChomozygous67084555
117902900379029004CT15GENIChomozygous67084557