chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124105848541058486GA46GENIChomozygous50205307
124105914941059150CCTGCAGA15GENIChomozygous50205308
124105915041059151GT20GENICheterozygous50205309
124105925141059252AAAT26GENICpossibly homozygous50205310
124105925241059253AAT24GENIChomozygous50205311
124105925341059254GT3GENIChomozygous50205312
124105925341059254GGA23GENIChomozygous50205313
124105969641059697CA43GENIChomozygous50205314
124106015641060157AG26GENIChomozygous50205315
124106050341060509AAAAGA------23GENIChomozygous50205316
124106076541060766GA20GENIChomozygous50205317
124106100841061009CCTCGTCG19GENIChomozygous50205318
124106102041061021AG23GENICheterozygous50422983
124106130141061302GA31GENIChomozygous50205319
124106185441061855T-44GENIChomozygous50205321
124106227041062271G-37GENIChomozygous50205322
124106232241062323TC35GENIChomozygous50205323
124106238441062385AG36GENICpossibly homozygous50205324
124106244141062442GA44GENIChomozygous50205325
124106364441063645GA41GENICpossibly homozygous50205326
124106385741063858GA26GENIChomozygous50205327
124106483341064834AG40GENIChomozygous50205328
124106500141065002AT37GENIChomozygous50205329
124106500541065006AT40GENIChomozygous50205330
124106564041065641CT51GENIChomozygous50205331
124106670441066705A-24GENICpossibly homozygous50205332
124106722641067227A-51GENIChomozygous50205333
124106742441067425TTA22GENIChomozygous50205334
124106742741067428AAATAT1GENIChomozygous50205335
124106744941067450G-10GENIChomozygous50205337
124106746341067464CT13GENIChomozygous50323726
124106746841067469C-10GENIChomozygous50205338
124106747841067479GA15GENIChomozygous50205339
124106748541067486TC15GENIChomozygous50205340
124106748941067490CG14GENIChomozygous50205341
124106749441067495CT18GENIChomozygous50205342
124106781241067813TC20GENIChomozygous50205343
124107692541076926TA22GENICpossibly homozygous50205346
124107692741076928TA20GENIChomozygous50205347
124107695341076954TA20GENICheterozygous50205349