chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2206928946206928947TC35GENIChomozygous111161307
2206929083206929084GC23GENIChomozygous110216594
2206929134206929135CT18GENIChomozygous111161309
2206929524206929525TC21GENIChomozygous110216595
2206934852206934853GA20GENIChomozygous111161311
2206935463206935464GA21GENIChomozygous111161313
2206935662206935663AG24GENIChomozygous110216598
2206936229206936230GT36GENIChomozygous111161315
2206937543206937544AG17GENIChomozygous111161317
2206943289206943290CT30GENIChomozygous111161321
2206944489206944490GA24GENIChomozygous111161323
2206944505206944506CG27GENIChomozygous111161325
2206945840206945841GT33GENIChomozygous110216603
2206945842206945843AT32GENIChomozygous110216604
2206948100206948101AG23GENIChomozygous110216606
2206954894206954895GC10GENIChomozygous111161329
2206956543206956544AC20GENIChomozygous111161331
2206959734206959735GA25GENIChomozygous111161333
2206960108206960109GA21GENIChomozygous111161335
2206960143206960144GA21GENIChomozygous111161337
2206960609206960610GA22GENICpossibly homozygous111161339
2206960687206960688CT31GENIChomozygous111161341
2206964043206964044CT27GENIChomozygous111161343
2206964901206964902TC39GENIChomozygous110216617
2206965498206965499TC22GENIChomozygous110216618
2206965563206965564TC26GENIChomozygous110216619
2206969695206969696TG23GENIChomozygous111161345
2206972841206972842CT32GENIChomozygous111161351
2206975852206975853GA28GENIChomozygous111161353
2206976305206976306AG21GENIChomozygous110216631
2206976951206976952AG18GENIChomozygous110216632
2206980157206980158CT23GENIChomozygous111161357
2206981389206981390GA7GENIChomozygous120460180
2206981580206981581CA18GENIChomozygous111161359
2206982122206982123TC22GENIChomozygous110216637
2206983655206983656AG24GENIChomozygous110216639
2206985251206985252AG12GENIChomozygous110216641
2206988830206988831AG23GENIChomozygous110216643
2206989150206989151AG30GENIChomozygous110216645
2206989157206989158CG32GENIChomozygous110216646