chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796683817966839CA24GENIChomozygous51628830
101796737917967380CCG29GENIChomozygous51628831
101796740017967401AAC25GENIChomozygous51335291
101796760517967606AATAACCTAGG37GENIChomozygous51335295
101796932017969321TTA31GENICpossibly homozygous51335300
101796932017969321TTAA31GENICheterozygous51815631
101796973417969735GA32GENIChomozygous51628834
101797013617970137GA26GENIChomozygous51628835
101797045117970452CCCAAACT31GENIChomozygous51335302
101797057017970571TTA24GENIChomozygous51335303
101797060617970607G-25GENIChomozygous51335304
101797061017970611TTA26GENIChomozygous51335305
101797061517970616A-25GENIChomozygous51335306
101797062017970621TTA24GENIChomozygous51335307
101797103517971036TC31GENIChomozygous51335312
101797116717971168GA35GENIChomozygous51628836
101797146517971466GA34GENIChomozygous51628837
101797193617971937AG15GENIChomozygous51335319
101797196417971966AA--13GENIChomozygous51628838
101797214517972147AC--32GENIChomozygous51335324
101797259117972592TTA37GENIChomozygous51335329
101797259217972593CT35GENIChomozygous52313695
101797271017972711CT41GENIChomozygous51628839
101797277217972773GT37GENIChomozygous51628840
101797282317972824TC41GENIChomozygous51335333
101797300217973003T-39GENIChomozygous51335334
101797326917973270AG43GENIChomozygous51628841
101797549417975495AG5GENIChomozygous51628842