chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179026664890266649TC17GENIChomozygous111286972
179026765490267655GA27GENIChomozygous111286974
179027010390270104AT20GENIChomozygous111141798
179027094290270943CT12GENICheterozygous111402011
179027313690273137CA17GENICheterozygous111402012
179027431190274312GA13GENIChomozygous111286976
179027716690277167CT23GENIChomozygous111286978
179027943890279439GA15GENIChomozygous111141800
179028861590288616AT10GENIChomozygous111141802
179028861790288618TG10GENIChomozygous111141804
179028874690288747CA18GENIChomozygous111141806
179029305990293060CT15GENIChomozygous111286980
179029375690293757CT13GENIChomozygous111286982
179029398390293984CT26GENIChomozygous111286984
179029558690295587CT17GENIChomozygous111286986
179029941590299416CT14GENICpossibly homozygous111286988
179030019490300195AG23GENIChomozygous111141811
179030019590300196AG23GENIChomozygous111141813
179030068090300681CT10GENIChomozygous111370737
179030631590306316TC21GENIChomozygous111286990
179030671090306711CT23GENIChomozygous111286992
179030978890309789TC17GENIChomozygous111141823
179031088190310882CT22GENIChomozygous111286994