chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160394685160394686GA17GENIChomozygous114074195
5160394781160394782TC17GENIChomozygous114074196
5160395004160395005TC17GENIChomozygous114074197
5160395804160395805CT16GENIChomozygous114074199
5160395890160395891CG19GENIChomozygous114074200
5160395896160395897TC19GENIChomozygous114074201
5160396095160396096AG24GENIChomozygous114074202
5160396109160396110GA22GENICpossibly homozygous114074203
5160396143160396144AC17GENIChomozygous114074204
5160396145160396146GA17GENIChomozygous114074205
5160396149160396150AG17GENIChomozygous114160901
5160396166160396167CT13GENIChomozygous114074206
5160396477160396478GA24GENIChomozygous114259574
5160396506160396507AC27GENIChomozygous114074207
5160396961160396962TC15GENIChomozygous114074209
5160398250160398251AG15GENIChomozygous114074211
5160398632160398633TC27GENICheterozygous114074212
5160398679160398680CG15GENIChomozygous114074213
5160398681160398682GA15GENICpossibly homozygous114160902
5160399256160399257TA5GENIChomozygous114074214
5160399800160399801CT24GENIChomozygous114074215
5160401780160401781AC5GENIChomozygous114074216
5160401873160401874AG6GENIChomozygous114074217
5160402867160402868CT22GENIChomozygous114259576