chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159521044159521045CG31GENIChomozygous55813489
5159521153159521154AG20GENIChomozygous55813491
5159521159159521160AG25GENIChomozygous55813492
5159522862159522863CT19GENIChomozygous55813494
5159523213159523214CT22GENIChomozygous55813496
5159523624159523625AT16GENIChomozygous55813498
5159523694159523695CT16GENIChomozygous55813500
5159523734159523735GA10GENIChomozygous55813501
5159524164159524165TC5GENIChomozygous55813503
5159524275159524276TC14GENIChomozygous55813505
5159524306159524307A-14GENIChomozygous55813507
5159524308159524311ATA---14GENICheterozygous55813509
5159524362159524363CT13GENIChomozygous55813511
5159524403159524408GCCCC-----21GENIChomozygous55813513
5159524764159524765GC18GENIChomozygous55813516
5159525078159525079CA20GENIChomozygous55813518
5159526063159526064GA17GENIChomozygous55813526
5159526131159526132GA22GENIChomozygous55813528
5159526206159526207AG30GENIChomozygous55813530
5159526278159526279AAG4GENIChomozygous56462794
5159526026159526027GGA2GENIChomozygous56462791
5159526034159526035GGAAGGAAAGAAAGAAAGAAAGAACTCTTCACCACT2GENIChomozygous56462792
5159526037159526038GGACTGTCTCAAAGAAA2GENIChomozygous56462793
5159526280159526281AAAGGAAGG4GENIChomozygous56462795
5159527045159527046G-13GENIChomozygous55813538
5159527503159527504CG29GENIChomozygous55813540
5159528027159528028CCAATAAT1GENIChomozygous56462796
5159528132159528133GA7GENIChomozygous55813542