chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796760517967606AATAACCTAGG26GENIChomozygous51335295
101796874617968747GA25GENIChomozygous51815629
101796932017969321TTA21GENICheterozygous51335300
101796932017969321TTAA21GENICpossibly homozygous51815631
101796965617969657TC39GENIChomozygous51815633
101796970817969709AC37GENIChomozygous51815635
101797045117970452CCCAAACT33GENIChomozygous51335302
101797057017970571TTA30GENIChomozygous51335303
101797060617970607G-34GENIChomozygous51335304
101797061017970611TTA34GENIChomozygous51335305
101797061517970616A-32GENIChomozygous51335306
101797062017970621TTA30GENIChomozygous51335307
101797103517971036TC25GENIChomozygous51335312
101797140917971410CT28GENICpossibly homozygous51815637
101797185017971851CT30GENIChomozygous51815639
101797193617971937AG26GENIChomozygous51335319
101797196317971964CCA16GENICpossibly homozygous51815641
101797214517972147AC--25GENIChomozygous51335324
101797234217972343AC14GENIChomozygous51815643
101797259117972592TTA30GENIChomozygous51335329
101797259217972593CT29GENIChomozygous52313695
101797282317972824TC32GENIChomozygous51335333
101797300217973003T-23GENIChomozygous51335334
101797441117974412GA26GENIChomozygous51815645
101797549417975495AG10GENIChomozygous51628842