chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796683217966833TTC14GENIChomozygous52117677
101796737917967380CCG16GENIChomozygous51628831
101796739917967400AAC18GENIChomozygous51628832
101796760517967606AATAACCTAGG27GENIChomozygous51335295
101796875017968751TTA15GENICpossibly homozygous52117679
101796932017969321TTA14GENIChomozygous51335300
101796973417969735GA20GENIChomozygous51628834
101797045117970452CCCAAACT20GENIChomozygous51335302
101797057017970571TTA13GENIChomozygous51335303
101797060617970607G-16GENIChomozygous51335304
101797061017970611TTA16GENIChomozygous51335305
101797061517970616A-14GENIChomozygous51335306
101797062017970621TTA14GENIChomozygous51335307
101797103517971036TC23GENIChomozygous51335312
101797116717971168GA18GENIChomozygous51628836
101797146517971466GA21GENIChomozygous51628837
101797193617971937AG13GENIChomozygous51335319
101797214517972147AC--16GENIChomozygous51335324
101797259117972592TTA15GENIChomozygous51335329
101797259217972593CT15GENIChomozygous52313695
101797277217972773GT16GENIChomozygous51628840
101797282317972824TC22GENIChomozygous51335333
101797300217973003T-20GENIChomozygous51335334
101797326917973270AG13GENIChomozygous51628841
101797549417975495AG26GENIChomozygous51628842