chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103533621235336213CA22GENIChomozygous52137669
103533664535336646AC32GENIChomozygous51407421
103533665935336660TTA24GENIChomozygous51407424
103533666035336661TTC24GENICpossibly homozygous51407427
103533666035336661TA25GENICheterozygous52137671
103533678535336786CT9GENIChomozygous51407430
103533720135337202GGT1GENIChomozygous51407432
103535219135352192AG14GENIChomozygous51407435
103535288635352887GGAC18GENICheterozygous51407437
103535289035352891CCAG31GENICheterozygous51407439
103535289235352893CG33GENICheterozygous51407441
103535296935352970AAT31GENIChomozygous51407443
103535727535357276CT34GENIChomozygous51407445
103535759135357592T-19GENICheterozygous51407447
103535813935358140CG24GENICheterozygous51407449
103535814335358144CG23GENICpossibly homozygous51634285
103535822435358225C-15GENICheterozygous51407451
103535823835358240TG--12GENICheterozygous51407453
103535824135358242CCTG14GENICheterozygous51407455
103535909035359091T-25GENIChomozygous51407457
103535979235359793T-31GENIChomozygous51407459
103535987935359880AG30GENIChomozygous51407461
103536005435360055AG22GENIChomozygous51407463
103536040035360401TC33GENIChomozygous51407465
103536179435361795CT20GENIChomozygous51407466
103536276535362767TT--10GENIChomozygous51407470
103536334335363344G-27GENICpossibly homozygous51407472
103536334635363349TTG---28GENIChomozygous51407474
103536334835363349G-30GENIChomozygous51407476
103536349935363500CT19GENIChomozygous51407478
103536470935364714AGTTT-----35GENIChomozygous51407480
103536603835366039AAAG29GENIChomozygous51407482
103536657735366578AG15GENIChomozygous51407484
103536931335369314GA23GENIChomozygous51407486
103536963235369633GGTT14GENIChomozygous51407488
103536963335369634TTTA14GENIChomozygous51407490
103537262335372624TA30INTERGENIChomozygous51407494