chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109095809090958091AAG12GENIChomozygous746096820
109095810390958104CG12GENIChomozygous632277985
109095887390958874AG24GENIChomozygous632277986
109095954790959548CG29GENIChomozygous632277987
109095954890959549CT29GENIChomozygous632277988
109095958890959589AG26GENIChomozygous632277989
109095967390959683TGGGGACGTT----------25GENIChomozygous746096821
109095972790959728AG24GENIChomozygous632277990
109096167690961677AC35GENIChomozygous632277991
109096226190962262AG29GENICpossibly homozygous632277992
109096300590963006CG39GENIChomozygous632277993
109096337490963375GC26GENIChomozygous632277994
109096401290964016AAAA----35GENIChomozygous746096822
109096401790964018AT34GENIChomozygous632277995
109096403590964036TTG21GENICpossibly homozygous746096823
109096404590964046TTGTGTGC30GENICpossibly homozygous746096824
109096406290964063TG41GENIChomozygous632277996
109096431890964319CT52GENICpossibly homozygous632277997
109096446390964464TTAA26GENICpossibly homozygous746096825
109096451490964525TTTTGGGGTTC-----------6GENICheterozygous746096826
109096495590964956CA53GENIChomozygous632277998
109096502090965022TG--26GENICheterozygous746096829
109096556890965569CT35GENICpossibly homozygous632277999
109096557890965579CCA34GENIChomozygous746096832
109096561690965617TTAC27GENICpossibly homozygous746096833
109096561690965617TTACACACACACACACACACAC27GENICheterozygous746096835
109096592290965923TA28GENIChomozygous632278000
109096610190966102TC17GENIChomozygous632278001
109096625590966256CT28GENIChomozygous632278002
109096643190966432CCTTTTTTTTT9GENIChomozygous746096838
109096649290966493C-21GENIChomozygous746096839
109096692790966936TTTTTTTTT---------13GENICpossibly homozygous746096840
109096695290966953TC28GENICpossibly homozygous632278003
109096699790966998A-30GENIChomozygous746096842
109096795190967952TG33GENIChomozygous632278004
109096807790968078AG27GENIChomozygous632278005