chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15109308013109308014TC74GENICheterozygous112643250
15109308226109308227TC48GENIChomozygous112643252
15109308616109308617GA41GENIChomozygous113072485
15109310821109310822TA53GENIChomozygous112643258
15109312408109312409TG45GENIChomozygous112643260
15109309035109309036CT45GENIChomozygous112865799
15109311424109311425AG44GENIChomozygous112865801
15109315258109315259GA52GENIChomozygous112865803
15109320351109320352AG51GENIChomozygous112865805
15109321661109321662CA26GENIChomozygous112643271
15109322641109322642CT30GENIChomozygous112643273
15109323166109323167GA50GENIChomozygous112865807
15109323596109323597AG44GENIChomozygous112643275
15109323953109323954AG53GENIChomozygous112865809
15109324146109324147AG61GENICpossibly homozygous112865811
15109324464109324465TG45GENIChomozygous112643277
15109328008109328009CG41GENICheterozygous112967869
15109328016109328017CG44GENICheterozygous119005460
15109328024109328025CG49GENICheterozygous119005461
15109328430109328431AG63GENIChomozygous112643281
15109330333109330334CT57GENIChomozygous112643285
15109331049109331050TC34GENIChomozygous112643287
15109331084109331085CT41GENIChomozygous112865813
15109332610109332611TC42GENIChomozygous112865815
15109335512109335513AT39GENIChomozygous112643295
15109336024109336025AG63GENICheterozygous118938743
15109328030109328031GC51GENICheterozygous118938737
15109328070109328071GC47GENICheterozygous118938738
15109335998109335999AG61GENICheterozygous118938740
15109336005109336006GA61GENICheterozygous118938741
15109336009109336010GA60GENICheterozygous118938742
15109334154109334155CT48GENIChomozygous112881329
15109336345109336346AG62GENICheterozygous118938744
15109336357109336358GA65GENICheterozygous118938745
15109336366109336367AG57GENICheterozygous118938746
15109336378109336379GA57GENICheterozygous118938747
15109336464109336465AG59GENIChomozygous112967875
15109336622109336623CA69GENIChomozygous113149801