chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160394685160394686GA34GENIChomozygous114074195
5160394781160394782TC42GENIChomozygous114074196
5160395004160395005TC37GENIChomozygous114074197
5160395013160395014CT35GENICpossibly homozygous114074198
5160395804160395805CT33GENIChomozygous114074199
5160395890160395891CG37GENIChomozygous114074200
5160395896160395897TC37GENIChomozygous114074201
5160396095160396096AG41GENIChomozygous114074202
5160396109160396110GA37GENIChomozygous114074203
5160396143160396144AC31GENIChomozygous114074204
5160396145160396146GA31GENIChomozygous114074205
5160396149160396150AG30GENIChomozygous114160901
5160396166160396167CT26GENIChomozygous114074206
5160396506160396507AC33GENIChomozygous114074207
5160396961160396962TC52GENIChomozygous114074209
5160397071160397072GA31GENIChomozygous114074210
5160398250160398251AG35GENIChomozygous114074211
5160398632160398633TC18GENICpossibly homozygous114074212
5160398679160398680CG32GENICheterozygous114074213
5160399256160399257TA13GENIChomozygous114074214
5160399800160399801CT39GENICpossibly homozygous114074215
5160401780160401781AC19GENIChomozygous114074216
5160401873160401874AG27GENIChomozygous114074217
5160401668160401669GT13GENICheterozygous114452669