chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7134591034134591035AG6GENIChomozygous115914270
7134591187134591188AC29GENIChomozygous115914272
7134591340134591341GA29GENIChomozygous115914274
7134591956134591957TA26GENIChomozygous115914276
7134593340134593341GA18GENIChomozygous115914278
7134593579134593580AT27GENIChomozygous115914280
7134593776134593777AC31GENIChomozygous115914282
7134595299134595300TC24GENIChomozygous115914284
7134597048134597049TG28GENIChomozygous115914286
7134597498134597499CT21GENIChomozygous115914288
7134598225134598226TC34GENIChomozygous115914290
7134598818134598819CT17GENIChomozygous115914292
7134599044134599045CA15GENIChomozygous115914294
7134599624134599625GC25GENIChomozygous115914296
7134599647134599648CT20GENIChomozygous115914298
7134599656134599657GC18GENIChomozygous115914300
7134599760134599761TA18GENIChomozygous115914302
7134600238134600239TC25GENIChomozygous115914304
7134600867134600868TA22GENIChomozygous115914306
7134600881134600882GA22GENIChomozygous115914308
7134601341134601342AT14GENIChomozygous115914310
7134602078134602079GA33GENIChomozygous115914312