chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154189809154189810GA22GENIChomozygous108316217
1154190590154190591CT27GENIChomozygous109519523
1154191408154191409CT32GENIChomozygous108316219
1154192988154192989TC16GENIChomozygous108316227
1154193672154193673AC29GENIChomozygous108316229
1154193826154193827TC10GENIChomozygous109519524
1154193874154193875CG8GENIChomozygous108316231
1154193875154193876GT8GENIChomozygous120506760
1154194066154194067TC21GENIChomozygous108316235
1154196597154196598TC24GENIChomozygous108316243
1154198977154198978CT21GENIChomozygous109519526
1154200087154200088GT29GENIChomozygous109519527
1154200428154200429GA21GENIChomozygous108316251
1154201360154201361CT30GENIChomozygous108316255
1154201418154201419GA17GENIChomozygous109519528
1154203043154203044AG24GENIChomozygous108316259
1154205548154205549TC14GENIChomozygous108316263
1154206141154206142TC17GENIChomozygous108316265
1154207192154207193AG19GENIChomozygous108316267
1154207368154207369AT31GENIChomozygous109519529
1154207745154207746AG28GENIChomozygous108316269
1154208340154208341TC26GENIChomozygous108316271
1154208764154208765GA14GENIChomozygous108316273
1154209739154209740GA14GENIChomozygous109519530
1154209834154209835GA13GENIChomozygous109519531
1154209929154209930TG6GENIChomozygous120506761
1154210492154210493TC29GENIChomozygous108316275
1154211406154211407CT25GENIChomozygous109519532
1154211421154211422GA28GENIChomozygous108316277
1154212990154212991GC15GENIChomozygous108316281
1154213335154213336AG17GENIChomozygous108316283
1154214183154214184GA19GENIChomozygous108316284
1154214207154214208TC18GENIChomozygous108316286
1154214413154214414TA8GENIChomozygous108316288