chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135526698255266983GT23GENIChomozygous976872289
135526700255267003GA28GENIChomozygous976872290
135526797155267972AC6GENIChomozygous976872291
135527074455270745GT23GENIChomozygous976872292
135527093955270940TC30GENIChomozygous976872293
135527108355271084GT37GENIChomozygous976872294
135527108955271090GA38GENIChomozygous976872295
135527110555271106GC37GENIChomozygous976872296
135527141355271414TC34GENIChomozygous976872297
135527143255271433AG32GENIChomozygous976872298
135527170555271706GT21GENIChomozygous976872299
135527182555271826CT31GENIChomozygous976872300
135527186055271861CG30GENIChomozygous976872301
135527198355271984TA24GENIChomozygous976872302
135527210355272104AG17GENIChomozygous976872303
135527216155272162AG16GENIChomozygous976872304
135527265155272652AG20GENIChomozygous976872305
135527265555272656AC18GENIChomozygous976872306
135527285655272857AG11GENIChomozygous976872307
135527329955273300CT11GENIChomozygous976872308
135527372555273726AC32GENIChomozygous976872309
135527631055276311GA35GENIChomozygous976872310
135528086855280869GA11GENIChomozygous976872311
135528155455281555GA22GENIChomozygous976872312
135528363155283632TC16GENIChomozygous976872313
135528406455284065CT16GENIChomozygous976872314
135528576055285761GT23GENIChomozygous976872315