chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118305259083052591TG20GENIChomozygous50848654
118305261683052617TC24GENIChomozygous50848655
118305352883053529TC32GENIChomozygous50848656
118305482283054823AAT22GENIChomozygous50848657
118305541583055416CT11GENIChomozygous50848658
118305695683056958AT--1GENIChomozygous50848659
118305711983057120CG19GENIChomozygous50848660
118305743783057438CT20GENIChomozygous50848661
118305856883058569CCTA3GENIChomozygous50848662
118306119683061197TC20GENIChomozygous50848664
118306172183061722GC27GENIChomozygous50848665
118306289083062891GA19GENIChomozygous50848666
118306452983064530G-15GENIChomozygous50848667
118306453683064537GT17GENIChomozygous50848668
118306455083064551G-15GENIChomozygous50848669
118306456183064562GA14GENIChomozygous50848670
118306456583064566GA14GENIChomozygous50848671
118306457483064575GA18GENIChomozygous50848672
118306457583064576GA18GENIChomozygous50848673
118306458383064584GA18GENIChomozygous50848674
118306461983064620GT18GENIChomozygous50848675
118306608883066089GGA14GENICheterozygous50848676
118306610183066102CA14GENIChomozygous50848678
118306654083066541AG21GENIChomozygous50848679
118306881483068815GGT11GENIChomozygous50848680
118306917983069180GGT11GENICheterozygous50848681
118306917983069180GGTT11GENICheterozygous51197446
118307132883071329GGTTT9GENIChomozygous50848682
118305985783059877GAGAGAGAGAGAGAGAGAGA--------------------4GENIChomozygous51191447
118306441983064420TTATTCATAGTCATGCTGCCCTTCAGGCAATGTTAAAGTCATGCTGAACATGATGTAGCTTGAAAGC23GENIChomozygous51191448