chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154189809154189810GA29GENIChomozygous108316217
1154191408154191409CT35GENIChomozygous108316219
1154192446154192447TG38GENIChomozygous108316221
1154192752154192753GA20GENIChomozygous108316223
1154192753154192754CT19GENIChomozygous108316225
1154192988154192989TC27GENIChomozygous108316227
1154193672154193673AC79GENIChomozygous108316229
1154193874154193875CG33GENIChomozygous108316231
1154194043154194044CT28GENIChomozygous108316233
1154194066154194067TC23GENIChomozygous108316235
1154195380154195381AG27GENIChomozygous108316237
1154196124154196125CA32GENIChomozygous108316239
1154196354154196355CT44GENIChomozygous108316241
1154196597154196598TC22GENIChomozygous108316243
1154200335154200336GA43GENIChomozygous108316249
1154200428154200429GA34GENIChomozygous108316251
1154201360154201361CT33GENIChomozygous108316255
1154202289154202290TC30GENIChomozygous108316257
1154203043154203044AG29GENIChomozygous108316259
1154205548154205549TC30GENIChomozygous108316263
1154206141154206142TC52GENIChomozygous108316265
1154207192154207193AG38GENIChomozygous108316267
1154207745154207746AG50GENIChomozygous108316269
1154208764154208765GA52GENIChomozygous108316273
1154210492154210493TC40GENIChomozygous108316275
1154211421154211422GA25GENIChomozygous108316277
1154211596154211597CT33GENIChomozygous108316279
1154212990154212991GC27GENIChomozygous108316281
1154213335154213336AG9GENIChomozygous108316283
1154214183154214184GA41GENIChomozygous108316284
1154214207154214208TC37GENIChomozygous108316286
1154214413154214414TA28GENIChomozygous108316288
1154215502154215503TC55GENIChomozygous108316290