chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5168601427168601428CT2GENIChomozygous56083142
5168602406168602407TC13GENICpossibly homozygous56083143
5168602567168602568AT7GENICpossibly homozygous56083145
5168602977168602978CT30GENICpossibly homozygous56083147
5168603783168603784TC15GENICpossibly homozygous56083148
5168603833168603834AG15GENIChomozygous56083149
5168604669168604670AC17GENICpossibly homozygous56083151
5168605120168605121AC19GENIChomozygous56083152
5168605246168605247TTTG21GENIChomozygous56083153
5168605921168605922AT12GENICheterozygous56083154
5168606840168606841AG13GENICheterozygous56083155
5168609217168609218GC6GENICheterozygous56364542
5168609500168609501CG5GENICheterozygous56364544
5168610646168610647G-9GENICpossibly homozygous56083160
5168610801168610802G-16GENIChomozygous56364545
5168610983168610984GA13GENICpossibly homozygous56083161
5168611564168611565TC17GENICheterozygous56083163
5168611934168611937TAT---5GENICheterozygous56083164
5168611976168611985CATCATCAG---------2GENIChomozygous57592841
5168612148168612149TC7GENIChomozygous56083166
5168612281168612282C-6GENIChomozygous56083167
5168613123168613124CT15GENIChomozygous56083168