chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15109308013109308014TC17GENICheterozygous112643250
15109308226109308227TC11GENIChomozygous112643252
15109308419109308420CT29GENIChomozygous112643254
15109309485109309486CT18GENIChomozygous112643256
15109310821109310822TA25GENIChomozygous112643258
15109312408109312409TG14GENIChomozygous112643260
15109312578109312579GA29GENICpossibly homozygous112643263
15109319840109319841CT14GENIChomozygous112643267
15109321661109321662CA10GENIChomozygous112643271
15109322641109322642CT5GENIChomozygous112643273
15109323596109323597AG14GENIChomozygous112643275
15109324464109324465TG11GENIChomozygous112643277
15109327209109327210TC27GENIChomozygous112643279
15109328430109328431AG32GENIChomozygous112643281
15109329939109329940GA14GENIChomozygous112643283
15109330333109330334CT13GENIChomozygous112643285
15109331049109331050TC15GENIChomozygous112643287
15109333823109333824TC21GENIChomozygous125783240
15109334159109334160CA15GENIChomozygous112643289
15109335090109335091CA26GENIChomozygous112643291
15109335171109335172GA14GENIChomozygous112643293
15109335512109335513AT16GENIChomozygous112643295
15109336464109336465AG14GENIChomozygous112967875
15109333142109333143CT4GENIChomozygous112768067