chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91576281115762812CT16GENIChomozygous667901466
91576362815763629GA9GENIChomozygous667901467
91576436615764367A-6GENICheterozygous767889790
91576591715765921GACG----8GENIChomozygous767889792
91576593815765939GC8GENIChomozygous667901468
91576622815766230GT--1GENIChomozygous767889794
91576633815766339CT5GENIChomozygous667901469
91576809615768097CT9GENIChomozygous667901470
91576896615768967GGGT6GENIChomozygous767889795
91576897115768973GG--6GENIChomozygous767889796
91577032815770329AAACACACACACAC3GENIChomozygous767889800
91577126815771269GT10GENIChomozygous667901471
91577278415772788CACA----2GENICheterozygous767889803
91577278615772788CA--2GENICheterozygous767889804
91577315615773160ACAT----13GENIChomozygous767889806
91577747015777471AG4GENIChomozygous667901472
91577867115778675GTGT----2GENIChomozygous767889811
91578202615782027AG9GENIChomozygous667901473
91578277515782776C-14GENIChomozygous767889814
91578281915782820C-19GENIChomozygous767889815
91578301015783013GGG---12GENICheterozygous767889816
91578301115783013GG--12GENICheterozygous767889817
91578309815783099T-10GENIChomozygous767889820
91578522615785230GTGT----4GENIChomozygous767889824
91578718915787190T-1GENIChomozygous767889827
91578757515787576T-3GENICheterozygous767889828
91578757715787578T-3GENICheterozygous767889829
91578979815789799AT1GENIChomozygous667901474
91578979915789800AT1GENIChomozygous667901475
91578980215789803AT1GENIChomozygous667901476
91578981115789812GT1GENIChomozygous667901477
91578981615789817GT1GENIChomozygous667901478
91579003815790039CCG1GENIChomozygous767889830
91579144115791442TC9GENIChomozygous667901479
91579790115797902CA7GENIChomozygous667901480
91579857515798576T-2GENIChomozygous767889831