chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139141A-4GENIChomozygous51601058
10110140004110140007AAA---14GENIChomozygous51601060
10110140015110140019AAAT----15GENIChomozygous51601061
10110140024110140025CT19GENIChomozygous51958641
10110140154110140155AG15GENIChomozygous51601062
10110140346110140347A-11GENIChomozygous51601063
10110140427110140428G-3GENIChomozygous51958644
10110140635110140636AG40GENIChomozygous51601064
10110142723110142725AA--20INTERGENIChomozygous51601067
10110142859110142860TC24INTERGENIChomozygous51601068
10110145251110145252AT37GENIChomozygous52273104
10110140048110140049AT16GENIChomozygous52273098
10110140436110140438GA--5GENIChomozygous52273100
10110142180110142181AT28INTERGENIChomozygous52273101
10110142493110142494CCT12INTERGENICpossibly homozygous52273102
10110142915110142920TTTTG-----14INTERGENIChomozygous52273103
10110145409110145410CT42GENIChomozygous52273105
10110145666110145667TC31GENIChomozygous51601069
10110146157110146158TG19GENIChomozygous52273106
10110147003110147004TTG15GENIChomozygous51601071
10110147010110147011C-17GENICheterozygous51601072
10110147657110147658CA31GENIChomozygous51601074
10110147827110147828AC27GENIChomozygous51601075
10110148207110148211AGAA----25GENIChomozygous52273107