chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108711712587117126CT22GENIChomozygous116817253
108711756287117563CT17GENIChomozygous116949046
108711787987117880CG14GENIChomozygous117197622
108711790387117904GT14GENIChomozygous117197624
108711810987118110TG35GENIChomozygous116817255
108711836487118365AG27GENIChomozygous116817257
108711843087118431AG25GENIChomozygous116817259
108711912187119122CT27GENIChomozygous116949048
108711931787119318AG32GENIChomozygous116817261
108711972587119726CG33GENIChomozygous116817263
108712002287120023CT33GENIChomozygous116817265
108712006987120070AC28GENIChomozygous116817267
108712033387120334CT30GENIChomozygous116817269
108712096087120961CT33GENIChomozygous116817271
108712118587121186CT29GENIChomozygous116817273
108712176187121762AT15GENIChomozygous116949052
108712199887121999CG36GENIChomozygous116817275
108712229387122294GA34GENIChomozygous116817277
108712235487122355TC26GENIChomozygous116817279
108712241387122414GA24GENIChomozygous116817281
108712350687123507TC15GENICpossibly homozygous116668893
108712191187121912TC21GENIChomozygous116668889
108712379987123800AT23GENIChomozygous116817283
108712427187124272GC29GENIChomozygous116817285
108712475387124754AG22GENIChomozygous116817287
108712519387125194AC17GENIChomozygous116817289
108712555187125552GC28GENIChomozygous116817291
108712578087125781CT26GENIChomozygous116817293
108712609387126094CT42GENIChomozygous116817295
108712640387126404CT40GENIChomozygous116817297
108712666287126663TG35GENIChomozygous116668895
108712691187126912TC22GENIChomozygous116668897
108712723587127236GT9GENIChomozygous117197626
108713054887130549CA25GENIChomozygous116817299
108713235087132351AG14GENIChomozygous116817301
108713357387133574GT15GENIChomozygous116817303
108713409587134096AG30GENIChomozygous116668933
108713537187135372AC36GENIChomozygous116668943
108713847987138480TC49GENIChomozygous116668947