chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101796683217966833TTC2GENIChomozygous52117677
101796737917967380CCG7GENIChomozygous51628831
101796739917967400AAC7GENIChomozygous51628832
101796760517967606AATAACCTAGG13GENIChomozygous51335295
101796875017968751TTA6GENIChomozygous52117679
101796932017969321TTA2GENIChomozygous51335300
101796973417969735GA12GENIChomozygous51628834
101797045117970452CCCAAACT4GENIChomozygous51335302
101797057017970571TTA4GENIChomozygous51335303
101797060617970607G-4GENIChomozygous51335304
101797061017970611TTA5GENIChomozygous51335305
101797061517970616A-4GENIChomozygous51335306
101797062017970621TTA7GENIChomozygous51335307
101797103517971036TC8GENIChomozygous51335312
101797116717971168GA15GENIChomozygous51628836
101797146517971466GA14GENIChomozygous51628837
101797193617971937AG7GENIChomozygous51335319
101797196317971964CCA5GENICheterozygous51815641
101797214517972147AC--10GENIChomozygous51335324
101797259117972592TTA6GENIChomozygous51335329
101797259217972593CT6GENIChomozygous52313695
101797277217972773GT8GENIChomozygous51628840
101797282317972824TC9GENIChomozygous51335333
101797300217973003T-6GENIChomozygous51335334
101797326917973270AG11GENIChomozygous51628841
101797549417975495AG7GENIChomozygous51628842