chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139141A-9GENICheterozygous51601058
10110140154110140155AG26GENIChomozygous51601062
10110140346110140347A-12GENIChomozygous51601063
10110140635110140636AG21GENIChomozygous51601064
10110142102110142103AC13INTERGENIChomozygous51958653
10110140024110140025CT26GENIChomozygous51958641
10110140427110140428G-4GENIChomozygous51958644
10110140631110140632GC20GENIChomozygous51958647
10110141338110141339CCG13GENICheterozygous51958650
10110142859110142860TC24INTERGENIChomozygous51601068
10110144375110144376AG14GENICheterozygous51958655
10110145666110145667TC21GENIChomozygous51601069
10110147003110147004TTG19GENIChomozygous51601071
10110147010110147011C-19GENICheterozygous51601072
10110147057110147058CCTTTT11GENIChomozygous51958658
10110147376110147377TA19GENIChomozygous51958661
10110147657110147658CA22GENIChomozygous51601074
10110147827110147828AC24GENIChomozygous51601075
10110147935110147936GA31GENIChomozygous51958664
10110142724110142725A-20INTERGENIChomozygous51774840