chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105685174156851742AT17GENIChomozygous116935793
105685182756851828CA15GENIChomozygous117059972
105685214156852142GA24GENIChomozygous116935795
105685215856852159TC23GENIChomozygous116978107
105685230856852309GC20GENIChomozygous116935797
105685259956852600GA13GENIChomozygous116935799
105685320356853204TC21GENIChomozygous116935803
105685324156853242GA22GENIChomozygous116935805
105685302556853026TG27GENIChomozygous116784373
105685317256853173TG23GENIChomozygous116784375
105685347956853479A19GENICpossibly homozygous131094613
105685350156853502T22GENIChomozygous131094614
105685414856854149GA19GENIChomozygous116935807
105685498056854981AT23GENIChomozygous116935809
105685520756855208AG15GENIChomozygous116935811
105685567756855678GC23GENIChomozygous116935813
105685596856855969AG21GENIChomozygous116784381
105685620356856204GA24GENIChomozygous116935815
105685663356856634TC30GENIChomozygous116935817
105685695456856955AG17GENIChomozygous116935823
105685732856857329TG16GENIChomozygous116935827
105685758156857582AG27GENIChomozygous116784389
105685780756857808GA14GENIChomozygous117059974
105685846856858469AG23GENIChomozygous116784391
105685881456858815CT19GENIChomozygous116935829
105685958056859581TC17GENIChomozygous116784393
105686033756860338CT13GENIChomozygous116935831
105686225856862259TA21GENIChomozygous116784397
105686320056863201AG19GENIChomozygous116978109
105686354756863548TC12GENIChomozygous117059976
105686357856863579AG13GENIChomozygous116784401
105686358556863586CT15GENIChomozygous117059978