chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166248633262486333GA93GENICheterozygous119169304
166248636862486369CT106GENICheterozygous119169306
166248640062486401TC104GENICheterozygous119121067
166248919762489198GT39GENICpossibly homozygous119121068
166251264862512649GA142GENICheterozygous119169308
166251266162512662AT160GENICheterozygous119169310
166251267062512671GC158GENICheterozygous119169313
166251268162512682AC180GENICheterozygous119121070
166251269962512700TC180GENICheterozygous119169315
166251270562512706CG186GENICheterozygous119121072
166251270862512709GA188GENICheterozygous119169318
166251271462512715TA185GENICheterozygous119121073
166251274962512750CA170GENICheterozygous119169320
166251275462512755TC160GENICheterozygous119121075
166251276162512762TC150GENICheterozygous119169322
166251278662512787GT100GENICheterozygous119169324
166251421762514218CT230GENICheterozygous119169326
166251421862514219AG200GENICheterozygous119169328
166251422962514230CA248GENICheterozygous119169330
166251425062514251GT231GENICheterozygous119121076
166251425262514253TC211GENICheterozygous119121077
166251426062514261TC218GENICheterozygous119121078
166251426362514264TC180GENICheterozygous119169332
166251426662514267TC205GENICheterozygous119121080
166251428662514287TC172GENICheterozygous119121081
166251431362514314GT134GENICheterozygous119121082
166251432162514322CT91GENICheterozygous119169334
166251440162514402GA68GENICheterozygous119169336
166251441762514418CT66GENICheterozygous119169338
166255444862554449TC55GENICheterozygous119121083
166258156162581562GC94GENICheterozygous119169340
166258159062581591CT111GENICheterozygous119169342
166258161062581611AT116GENICheterozygous119169344
166258161162581612GT116GENICheterozygous119169346
166258161362581614CT118GENICheterozygous119169348
166259351162593512AG48GENICheterozygous112068266