chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796683917966840CCG12GENIChomozygous52313694
101796737917967380CCG12GENIChomozygous51628831
101796739917967400AAC14GENIChomozygous51628832
101796760517967606AATAACCTAGG15GENIChomozygous51335295
101796875017968751TTA22GENIChomozygous52117679
101796932017969321TTA17GENICpossibly homozygous51335300
101796932017969321TTAA17GENICheterozygous51815631
101796973417969735GA22GENIChomozygous51628834
101797045117970452CCCAAACT12GENIChomozygous51335302
101797057017970571TTA16GENIChomozygous51335303
101797060617970607G-9GENIChomozygous51335304
101797061017970611TTA9GENIChomozygous51335305
101797061517970616A-8GENIChomozygous51335306
101797062017970621TTA9GENIChomozygous51335307
101797103517971036TC28GENIChomozygous51335312
101797116717971168GA20GENIChomozygous51628836
101797146517971466GA20GENIChomozygous51628837
101797193617971937AG12GENIChomozygous51335319
101797214517972147AC--17GENIChomozygous51335324
101797259117972592TTA13GENIChomozygous51335329
101797259217972593CT13GENIChomozygous52313695
101797277217972773GT17GENIChomozygous51628840
101797282317972824TC12GENIChomozygous51335333
101797300217973003T-25GENIChomozygous51335334
101797326917973270AG25GENIChomozygous51628841
101797549417975495AG10GENIChomozygous51628842