chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154189809154189810GA21GENIChomozygous108316217
1154191408154191409CT24GENIChomozygous108316219
1154192988154192989TC18GENIChomozygous108316227
1154193672154193673AC32GENIChomozygous108316229
1154193874154193875CG18GENIChomozygous108316231
1154193875154193876GT18GENIChomozygous120506760
1154194066154194067TC25GENIChomozygous108316235
1154196597154196598TC19GENIChomozygous108316243
1154190590154190591CT34GENIChomozygous109519523
1154193826154193827TC13GENIChomozygous109519524
1154198977154198978CT17GENIChomozygous109519526
1154200087154200088GT19GENIChomozygous109519527
1154200428154200429GA14GENIChomozygous108316251
1154201360154201361CT19GENIChomozygous108316255
1154201418154201419GA38GENIChomozygous109519528
1154203043154203044AG17GENIChomozygous108316259
1154205548154205549TC26GENIChomozygous108316263
1154206141154206142TC29GENIChomozygous108316265
1154207192154207193AG13GENIChomozygous108316267
1154207368154207369AT22GENIChomozygous109519529
1154207745154207746AG16GENIChomozygous108316269
1154208340154208341TC23GENIChomozygous108316271
1154208764154208765GA21GENIChomozygous108316273
1154209739154209740GA18GENIChomozygous109519530
1154209834154209835GA11GENIChomozygous109519531
1154209929154209930TG4GENIChomozygous120506761
1154210492154210493TC20GENIChomozygous108316275
1154211406154211407CT20GENIChomozygous109519532
1154211596154211597CT13GENIChomozygous108316279
1154212990154212991GC19GENIChomozygous108316281
1154213335154213336AG12GENIChomozygous108316283
1154214183154214184GA16GENIChomozygous108316284
1154214207154214208TC9GENIChomozygous108316286
1154214413154214414TA10GENIChomozygous108316288