chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105685174156851742AT21GENIChomozygous116935793
105685182756851828CA18GENIChomozygous117059972
105685214156852142GA8GENIChomozygous116935795
105685215856852159TC9GENIChomozygous116978107
105685230856852309GC19GENIChomozygous116935797
105685259956852600GA16GENIChomozygous116935799
105685320356853204TC12GENIChomozygous116935803
105685324156853242GA18GENIChomozygous116935805
105685414856854149GA9GENIChomozygous116935807
105685498056854981AT21GENIChomozygous116935809
105685520756855208AG11GENIChomozygous116935811
105685567756855678GC8GENIChomozygous116935813
105685596856855969AG6GENIChomozygous116784381
105685302556853026TG12GENIChomozygous116784373
105685317256853173TG11GENIChomozygous116784375
105685620356856204GA32GENIChomozygous116935815
105685663356856634TC15GENIChomozygous116935817
105685695456856955AG26GENIChomozygous116935823
105685732856857329TG24GENIChomozygous116935827
105685758156857582AG10GENIChomozygous116784389
105685780756857808GA20GENIChomozygous117059974
105685846856858469AG9GENIChomozygous116784391
105685881456858815CT15GENIChomozygous116935829
105685958056859581TC13GENIChomozygous116784393
105686033756860338CT22GENIChomozygous116935831
105686225856862259TA26GENIChomozygous116784397
105686354756863548TC13GENIChomozygous117059976
105686357856863579AG4GENIChomozygous116784401
105686358556863586CT7GENIChomozygous117059978