chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139142AA--7GENICheterozygous52410326
10110139141110139142A-7GENICheterozygous52684191
10110140015110140019AAAT----17GENIChomozygous51601061
10110140024110140025CT20GENIChomozygous51958641
10110140048110140049AT19GENIChomozygous52273098
10110140154110140155AG13GENIChomozygous51601062
10110140346110140347A-10GENIChomozygous51601063
10110140436110140438GA--5GENIChomozygous52273100
10110140635110140636AG26GENIChomozygous51601064
10110142180110142181AT28INTERGENIChomozygous52273101
10110142493110142494CCT10INTERGENICpossibly homozygous52273102
10110142723110142725AA--21INTERGENICpossibly homozygous51601067
10110142859110142860TC22INTERGENIChomozygous51601068
10110142915110142920TTTTG-----18INTERGENIChomozygous52273103
10110145251110145252AT29GENIChomozygous52273104
10110145409110145410CT40GENIChomozygous52273105
10110145666110145667TC22GENIChomozygous51601069
10110146157110146158TG17GENIChomozygous52273106
10110147657110147658CA20GENIChomozygous51601074
10110147827110147828AC26GENIChomozygous51601075
10110148207110148211AGAA----28GENIChomozygous52273107
10110142724110142725A-21INTERGENICheterozygous51774840