chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139141A-13GENICheterozygous51601058
10110140004110140007AAA---27GENIChomozygous51601060
10110140015110140019AAAT----31GENIChomozygous51601061
10110140154110140155AG47GENIChomozygous51601062
10110140346110140347A-36GENIChomozygous51601063
10110140635110140636AG39GENIChomozygous51601064
10110140024110140025CT37GENIChomozygous51958641
10110140427110140428G-4GENIChomozygous51958644
10110140048110140049AT38GENIChomozygous52273098
10110140436110140438GA--6GENIChomozygous52273100
10110142180110142181AT59INTERGENIChomozygous52273101
10110142493110142494CCT21INTERGENIChomozygous52273102
10110142723110142725AA--37INTERGENIChomozygous51601067
10110142859110142860TC43INTERGENICpossibly homozygous51601068
10110142915110142920TTTTG-----16INTERGENIChomozygous52273103
10110144375110144376AG49GENICheterozygous51958655
10110145251110145252AT39GENICpossibly homozygous52273104
10110145409110145410CT56GENICpossibly homozygous52273105
10110145666110145667TC41GENICpossibly homozygous51601069
10110147003110147004TTG27GENIChomozygous51601071
10110147010110147011C-28GENICheterozygous51601072
10110147657110147658CA55GENIChomozygous51601074
10110147827110147828AC55GENIChomozygous51601075
10110146157110146158TG60GENIChomozygous52273106
10110148207110148211AGAA----36GENIChomozygous52273107