chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129798708129798709CT23GENIChomozygous947311102
7129799658129799659GA24GENIChomozygous947311103
7129800613129800614CT15GENIChomozygous947311104
7129801117129801118AG7GENIChomozygous947311105
7129801936129801937GA10GENIChomozygous947311106
7129802004129802005GC7GENICheterozygous947311107
7129804694129804695TG24GENIChomozygous947311108
7129804776129804777TC26GENIChomozygous947311109
7129804821129804822GA22GENIChomozygous947311110
7129805161129805162TC18GENIChomozygous947311111
7129805282129805283AG23GENIChomozygous947311112
7129805315129805316TC18GENIChomozygous947311113
7129805327129805328GT18GENIChomozygous947311114
7129806000129806001CT22GENIChomozygous947311115
7129806589129806590CT34GENIChomozygous947311116
7129807333129807334GA19GENIChomozygous947311117
7129807636129807637CA7GENIChomozygous947311118
7129808777129808778CT23GENIChomozygous947311119
7129808911129808912GT30GENIChomozygous947311120
7129808987129808988AG30GENIChomozygous947311121
7129810320129810321TC28GENIChomozygous947311122
7129810349129810350TC19GENIChomozygous947311123
7129810795129810796CT23GENIChomozygous947311124
7129810829129810830GA26GENIChomozygous947311125
7129811223129811224AG32GENIChomozygous947311126