chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84921980449219805CCA31GENIChomozygous53111245
84922007449220075CT51GENIChomozygous53111247
84922130249221303AATT32GENIChomozygous52971550
84922237049222371GA25GENIChomozygous53111248
84922258449222585AG24GENICheterozygous52625300
84922258849222589CCAAAAAA12GENIChomozygous52971553
84922289449222895GGTAA27GENICpossibly homozygous53111249
84922289749222898GA32GENIChomozygous52971554
84922388349223884TC34GENIChomozygous52971558
84922434749224348A-40GENIChomozygous52971559
84922435549224358AAT---49GENIChomozygous53111251
84922469049224691GA37GENIChomozygous53111253
84922495349224954CT31GENIChomozygous52971563
84922495949224960CA33GENIChomozygous53111254
84922502649225027TC34GENIChomozygous52971565
84922564849225649TC42GENIChomozygous52971566
84922615549226156GT57GENIChomozygous52971567
84922639649226397AT25GENIChomozygous53111256
84922663149226632CT47GENIChomozygous52971571
84922794849227949TTC9GENIChomozygous52971573
84922795249227953G-10GENIChomozygous52625306
84922795449227956TT--10GENICpossibly homozygous52971574
84922835149228352TC35GENIChomozygous52971581
84922845249228453GA34GENIChomozygous52971582
84922889549228896CA31GENIChomozygous52971583
84922921449229220GAGAGA------7GENICpossibly homozygous52971584
84922929749229298GGGTGT17GENIChomozygous53111258
84922935749229358CCTG19GENIChomozygous53111260
84922937549229376CG35GENIChomozygous53111262
84922973249229733AC40GENIChomozygous52971586
84923005349230054GGT17GENICpossibly homozygous52971588
84923015149230152GA26GENICpossibly homozygous53111263
84923025849230260GG--23GENIChomozygous53111265
84923028449230286GT--22GENIChomozygous53111266
84923070049230701TC39GENIChomozygous53111268
84923072149230722GA40GENIChomozygous53111270
84923092249230927TCTAT-----24GENIChomozygous53111272
84923138249231383AG30GENIChomozygous53111274