chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139142AA--3GENICheterozygous52410326
10110140015110140019AAAT----11GENIChomozygous51601061
10110140154110140155AG11GENIChomozygous51601062
10110140346110140347A-13GENIChomozygous51601063
10110140635110140636AG21GENIChomozygous51601064
10110140024110140025CT13GENIChomozygous51958641
10110140048110140049AT9GENIChomozygous52273098
10110140436110140438GA--1GENIChomozygous52273100
10110142180110142181AT26INTERGENIChomozygous52273101
10110142493110142494CCT12INTERGENIChomozygous52273102
10110142723110142725AA--9INTERGENIChomozygous51601067
10110142859110142860TC10INTERGENIChomozygous51601068
10110142915110142920TTTTG-----11INTERGENIChomozygous52273103
10110145251110145252AT24GENIChomozygous52273104
10110145409110145410CT30GENIChomozygous52273105
10110145666110145667TC27GENIChomozygous51601069
10110146157110146158TG22GENIChomozygous52273106
10110147657110147658CA30GENIChomozygous51601074
10110147827110147828AC33GENIChomozygous51601075
10110148207110148211AGAA----32GENIChomozygous52273107