chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105983985559839856AG4INTERGENIChomozygous51466349
105984095759840958GC10INTERGENICpossibly homozygous51466350
105984462759844628TC6INTERGENIChomozygous51466351
105984567859845679CT10INTERGENIChomozygous51466352
105984616559846166GA4INTERGENICheterozygous51466355
105984670959846710CT6INTERGENICheterozygous51466357
105984670259846703C-7INTERGENICheterozygous52319607
105984767859847679TTA2INTERGENIChomozygous51466359
105984844259848443AC9INTERGENIChomozygous51466360
105985272659852727GA4INTERGENICheterozygous51466362
105986254559862548AGA---7INTERGENIChomozygous51466366
105988043059880431TC3INTERGENIChomozygous51466368
105988043459880435TC2INTERGENIChomozygous51466369
105988046759880468GGT1INTERGENIChomozygous51466370
105988066759880668CCGT9INTERGENICheterozygous52319609
105988078759880788TC20INTERGENICpossibly homozygous51466373
105988113859881139TG5INTERGENIChomozygous51466374
105988124059881241CA11INTERGENICheterozygous51466375
105988142159881422CT30INTERGENICpossibly homozygous51466376
105988184059881841CT9INTERGENIChomozygous51466377
105988197159881972GA27INTERGENIChomozygous51466378
105988207259882073AG20INTERGENIChomozygous51466379
105988278759882788CCA4INTERGENICheterozygous51466384
105988226459882265CT19INTERGENIChomozygous51466380
105988255359882554CG21INTERGENICpossibly homozygous51466383
105988291359882914AG13INTERGENIChomozygous51466385
105988302759883028CA19INTERGENIChomozygous51466386
105988316859883169AG9INTERGENIChomozygous51466387
105988387459883875TC9INTERGENIChomozygous51466389
105988507359885074C-12INTERGENIChomozygous51466390
105988551459885515CT10INTERGENIChomozygous51466391
105988768659887687TC17INTERGENICpossibly homozygous51466400
105988784859887849AG10INTERGENIChomozygous51466401