chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796683217966833TTC17GENIChomozygous52117677
101796737917967380CCG32GENIChomozygous51628831
101796739917967400AAC29GENIChomozygous51628832
101796760517967606AATAACCTAGG37GENIChomozygous51335295
101796875017968751TTA27GENIChomozygous52117679
101796932017969321TTA22GENIChomozygous51335300
101796973417969735GA36GENIChomozygous51628834
101797045117970452CCCAAACT30GENIChomozygous51335302
101797057017970571TTA23GENIChomozygous51335303
101797060617970607G-25GENIChomozygous51335304
101797061017970611TTA26GENIChomozygous51335305
101797061517970616A-26GENIChomozygous51335306
101797062017970621TTA24GENIChomozygous51335307
101797103517971036TC25GENIChomozygous51335312
101797116717971168GA32GENIChomozygous51628836
101797146517971466GA21GENIChomozygous51628837
101797193617971937AG16GENIChomozygous51335319
101797196317971964CCA7GENICheterozygous51815641
101797214517972147AC--23GENIChomozygous51335324
101797259117972592TTA31GENIChomozygous51335329
101797259217972593CT31GENIChomozygous52313695
101797277217972773GT27GENIChomozygous51628840
101797282317972824TC29GENIChomozygous51335333
101797300217973003T-27GENIChomozygous51335334
101797326917973270AG37GENIChomozygous51628841
101797549417975495AG21GENIChomozygous51628842