chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23018006630180066T14GENIChomozygous127607275
23018007330180074C14GENIChomozygous127607276
23018007630180077GA13GENIChomozygous120122962
23018008130180082CT14GENIChomozygous109672753
23018008430180084C13GENIChomozygous127607277
23018010030180101CT18GENIChomozygous109672755
23018200130182001G30GENIChomozygous127607278
23018329330183294T13GENIChomozygous127607279
23018837030188371AG5GENIChomozygous109672775
23018839930188400CT7GENIChomozygous109672777
23018873630188737TG27GENICheterozygous109672787
23018874030188741CT26GENICheterozygous109672789
23018875130188753AT27GENICheterozygous130739487
23018875730188760ATA26GENICheterozygous130739488
23018877730188778AG24GENICheterozygous110928677
23020155130201552CT16GENIChomozygous109672829
23020165830201662CCCC20GENIChomozygous127607283
23020166330201663AAT21GENIChomozygous127607284
23021354030213541CT36GENICheterozygous129874426
23021354230213543TA36GENICheterozygous129874427
23021356930213569AGCG36GENICheterozygous129863670
23020783130207832T2GENIChomozygous129863666
23020784730207848C9GENIChomozygous129863667
23020785530207855C11GENIChomozygous129863668
23020785730207864CCATAGA11GENIChomozygous129863669
23018978030189781TC21GENIChomozygous111098066
23020743330207434CT24GENIChomozygous134516889
23020784330207844AC9GENIChomozygous120165314
23021357530213576CA36GENICheterozygous110500777
23021363030213631GA31GENICheterozygous110500779
23021363130213632GT31GENICheterozygous110500781
23021363330213634TA31GENICheterozygous110500783
23021365230213653GA31GENICheterozygous109672863
23021365630213657AG30GENICheterozygous109672865
23021366130213662CT28GENICheterozygous109672867
23021366930213670GA30GENICheterozygous109672869
23023663630236637CT24GENIChomozygous120165315
23023451630234516GTG9GENICheterozygous130860654
23023378630233854ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA7GENIChomozygous130244041