chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182369569323695694TC20GENIChomozygous140286692
182369961823699619GA19GENIChomozygous140286695
182370023923700240TC18GENIChomozygous140286696
182370132123701321TATATTTGA33GENIChomozygous143661769
182370432223704323TC17GENIChomozygous140286698
182370460423704605TA14GENIChomozygous140286699
182371160723711608TC23GENIChomozygous140286704
182370461223704613AC15GENIChomozygous140286700
182370534023705341GA12GENIChomozygous140286701
182371041123710412GA23GENIChomozygous140286703
182370199423701995TA25GENIChomozygous143681033
182370439123704392AT20GENIChomozygous143681034
182370466723704668GA14GENIChomozygous143681035
182370693523706936AG22GENIChomozygous143681036
182370716723707168C13GENIChomozygous140215774
182371187623711877A18GENIChomozygous140215775
182371254823712549AT17GENIChomozygous143681037
182371342023713421AT16GENIChomozygous140286706
182371343923713439TG11GENIChomozygous140215776
182371451523714515TTC20GENIChomozygous140215777
182371517623715177AG21GENIChomozygous140286707
182371593823715939AG17GENIChomozygous140286708
182371754123717542TC27GENIChomozygous140286709
182371978023719780GTG26GENIChomozygous140215778
182372206723722068CT9GENIChomozygous140286712
182372207323722074GA8GENIChomozygous140286713
182372484923724850AG25GENIChomozygous143681038
182372489923724900GA26GENIChomozygous143681039
182372490023724901TC26GENIChomozygous140286714
182372581923725820TC22GENIChomozygous143681040
182372662523726628TAA31GENIChomozygous143661770
182372786023727861AG24GENIChomozygous140286715
182372966323729663GT24GENIChomozygous140215779
182372996823729968C28GENIChomozygous140215780
182373426023734261GA25GENIChomozygous140286719