chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706689247066893AG14GENIChomozygous961740253
104706738747067388TC28GENIChomozygous961740254
104706760647067607GA18GENIChomozygous961740255
104706850747068508AG19GENIChomozygous961740256
104708237347082374GA24GENIChomozygous961740257
104708308147083082GA23GENIChomozygous961740258
104708367247083673TC20GENIChomozygous961740259
104708432247084323AG14GENIChomozygous961740260
104708446147084462TC22GENIChomozygous961740261
104708510747085108GA28GENIChomozygous961740262
104708587347085874TC22GENIChomozygous961740263
104708642247086423GC24GENIChomozygous961740264
104708650047086501AG16GENIChomozygous961740265
104708655247086553CT12GENIChomozygous961740266
104708734847087349GA28GENIChomozygous961740267
104708819347088194GT33GENIChomozygous961740268
104709123347091234GA36GENIChomozygous961740269
104709128847091289GT34GENIChomozygous961740270
104709132947091330GA39GENIChomozygous961740271
104709153347091534CT23GENIChomozygous961740272
104709296347092964TC31GENIChomozygous961740273
104709340547093406AG36GENIChomozygous961740274
104709355047093551CA26GENIChomozygous961740275
104709355247093553TC24GENIChomozygous961740276
104709370847093709TC14GENIChomozygous961740277
104709401947094020TC14GENIChomozygous961740278
104709432547094326TA37GENIChomozygous961740279
104709540047095401AC22GENIChomozygous961740280
104709700447097005TC20GENIChomozygous961740281
104709953547099536TA18GENIChomozygous961740282
104710175847101759CT23GENIChomozygous961740283
104710472647104727GA36GENIChomozygous961740284
104710532847105329TC37GENIChomozygous961740285
104710603047106031TC26GENIChomozygous961740286
104710799847107999AG30GENIChomozygous961740287
104710810447108105CG22GENIChomozygous961740288
104711059447110595GC18GENIChomozygous961740289