chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC23GENIChomozygous563414948
102640292126402922AAT3GENIChomozygous707708855
102640309326403094TG8GENIChomozygous563414949
102640313226403133TC17GENIChomozygous563414950
102640317126403172TTCAGCTACTGCTCATTG4GENICheterozygous707708856
102640334626403347A-6GENIChomozygous707708857
102640471626404717AT21GENICpossibly homozygous565147820
102640495526404956CA14GENIChomozygous563414951
102640620426406205TC6GENIChomozygous565147821
102640705526407056GT8GENIChomozygous565147822
102640814826408149A-10GENIChomozygous707708858
102640920926409210TC18GENICpossibly homozygous563414952
102640978426409785CT13GENICpossibly homozygous565147823
102641041826410419AG5GENIChomozygous565147824
102641068126410682CT15GENIChomozygous565147825
102641118626411187TG10GENIChomozygous565147826
102641178826411789GT25GENICpossibly homozygous565147827
102641254626412547TC11GENIChomozygous565147828
102641324026413241GA6GENIChomozygous565147829
102641324726413248CA2GENIChomozygous565147830
102641456226414563T-13GENICpossibly homozygous707708859
102641481126414812AT2GENIChomozygous565147831
102641503726415038GC24GENICpossibly homozygous565147832
102641543426415435AG19GENICpossibly homozygous565147833
102641558826415589CT5GENIChomozygous565147834
102641586926415870GC11GENIChomozygous565147835
102641608926416090AATCTTT4GENIChomozygous707708861
102641661126416612TC20GENIChomozygous563414953
102641721826417219TC13GENICpossibly homozygous565147836
102641847526418476GC20GENICpossibly homozygous565147837
102641858826418589TG5GENICheterozygous565147838
102641859826418604AGTAAA------5GENIChomozygous707708862
102641860426418605AC4GENIChomozygous565147839
102641873326418734TG20GENIChomozygous565147840
102641894626418947CT5GENICheterozygous565147841
102641916626419167CT7GENICpossibly homozygous565147842
102641940326419404GA9GENIChomozygous565147843