chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15109308013109308014TC11GENICheterozygous112643250
15109308419109308420CT6GENIChomozygous112643254
15109309485109309486CT9GENIChomozygous112643256
15109310821109310822TA12GENIChomozygous112643258
15109312408109312409TG6GENIChomozygous112643260
15109312578109312579GA8GENIChomozygous112643263
15109316851109316852CT10GENIChomozygous112643265
15109320351109320352AT11GENIChomozygous112643269
15109321661109321662CA11GENIChomozygous112643271
15109322641109322642CT11GENIChomozygous112643273
15109323596109323597AG10GENIChomozygous112643275
15109324464109324465TG13GENIChomozygous112643277
15109327209109327210TC9GENIChomozygous112643279
15109328430109328431AG7GENIChomozygous112643281
15109329939109329940GA15GENIChomozygous112643283
15109330333109330334CT12GENIChomozygous112643285
15109331049109331050TC10GENIChomozygous112643287
15109334159109334160CA13GENIChomozygous112643289
15109335090109335091CA3GENIChomozygous112643291
15109335171109335172GA6GENIChomozygous112643293
15109335512109335513AT8GENIChomozygous112643295
15109333142109333143CT10GENIChomozygous112768067