chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139142AA--17GENICheterozygous52410326
10110140005110140007AA--17GENICpossibly homozygous52969658
10110140154110140155AG11GENIChomozygous51601062
10110140635110140636AG8GENIChomozygous51601064
10110140757110140758CA7GENIChomozygous52969660
10110141421110141422CT31INTERGENIChomozygous52969662
10110141590110141591GA34INTERGENIChomozygous52969664
10110142025110142026CG34INTERGENIChomozygous52969666
10110142723110142725AA--22INTERGENIChomozygous51601067
10110142859110142860TC22INTERGENIChomozygous51601068
10110145620110145621AG27GENIChomozygous52969668
10110145666110145667TC25GENIChomozygous51601069
10110147099110147100AATTTTTTTTTTTTT10GENICheterozygous52969671
10110147657110147658CA39GENIChomozygous51601074
10110147827110147828AC39GENIChomozygous51601075
10110147058110147059T-18GENIChomozygous52652003