chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108711712587117126CT21GENIChomozygous116817253
108711756287117563CT17GENIChomozygous116949046
108711810987118110TG9GENIChomozygous116817255
108711836487118365AG9GENIChomozygous116817257
108711912187119122CT25GENIChomozygous116949048
108711931787119318AG18GENIChomozygous116817261
108711972587119726CG16GENIChomozygous116817263
108712033387120334CT13GENIChomozygous116817269
108712096087120961CT9GENIChomozygous116817271
108712118587121186CT8GENIChomozygous116817273
108712176187121762AT17GENIChomozygous116949052
108712191187121912TC27GENIChomozygous116668889
108712199887121999CG21GENIChomozygous116817275
108712229387122294GA23GENIChomozygous116817277
108712241387122414GA18GENIChomozygous116817281
108712350687123507TC11GENIChomozygous116668893
108712379987123800AT18GENIChomozygous116817283
108712427187124272GC27GENIChomozygous116817285
108712475387124754AG33GENIChomozygous116817287
108712519387125194AC22GENIChomozygous116817289
108712555187125552GC23GENIChomozygous116817291
108712578087125781CT14GENIChomozygous116817293
108712609387126094CT24GENIChomozygous116817295
108712640387126404CT17GENIChomozygous116817297
108712666287126663TG20GENIChomozygous116668895
108712691187126912TC17GENIChomozygous116668897
108712722187127222TG5GENIChomozygous116668899
108713054887130549CA21GENICpossibly homozygous116817299
108713235087132351AG25GENIChomozygous116817301
108713357387133574GT28GENIChomozygous116817303
108713409587134096AG20GENIChomozygous116668933
108713537187135372AC16GENIChomozygous116668943
108713847987138480TC6GENIChomozygous116668947