chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110140015110140019AAAT----13GENIChomozygous51601061
10110140024110140025CT20GENIChomozygous51958641
10110140048110140049AT23GENIChomozygous52273098
10110140154110140155AG13GENIChomozygous51601062
10110140346110140347A-13GENIChomozygous51601063
10110140635110140636AG11GENIChomozygous51601064
10110142180110142181AT23INTERGENIChomozygous52273101
10110142493110142494CCT21INTERGENIChomozygous52273102
10110142723110142725AA--17INTERGENICpossibly homozygous51601067
10110142859110142860TC17INTERGENIChomozygous51601068
10110142915110142920TTTTG-----12INTERGENIChomozygous52273103
10110145251110145252AT15GENIChomozygous52273104
10110145409110145410CT10GENIChomozygous52273105
10110145666110145667TC15GENIChomozygous51601069
10110146157110146158TG24GENIChomozygous52273106
10110147657110147658CA27GENIChomozygous51601074
10110147827110147828AC13GENIChomozygous51601075
10110148207110148211AGAA----12GENIChomozygous52273107
10110142724110142725A-17INTERGENICheterozygous51774840