chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189286456189286457TC27GENIChomozygous110171270
2189287963189287964AC51GENIChomozygous110171272
2189288519189288520GA49GENIChomozygous110171274
2189289639189289640AG49GENIChomozygous110171276
2189290917189290918CT45GENIChomozygous110171278
2189293263189293263TTTTG15GENICheterozygous127717740
2189296717189296718GA36GENIChomozygous110171280
2189297602189297603AG39GENIChomozygous110171283
2189298374189298375GA39GENIChomozygous110171285
2189298936189298937TC52GENIChomozygous110171287
2189299140189299141GA45GENIChomozygous110171289
2189300435189300436GA36GENIChomozygous110171291
2189301250189301251AG37GENICpossibly homozygous110171293
2189303134189303135TC37GENIChomozygous110171295
2189303680189303681GC33GENIChomozygous110171296
2189293268189293269GT30GENIChomozygous120155238