chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103533546035335461CCAGCTACAGCGTACTTATATATAATAAATGAATAAATCTTTAAAAAAAAA14GENIChomozygous52367390
103533623135336232TG38GENIChomozygous51407419
103535288635352887GGACACAGACAC30GENICpossibly homozygous52647434
103535296935352970AAT36GENIChomozygous51407443
103535638735356388CCAAAAAAAAAAAAAAAA17GENIChomozygous52367392
103535727535357276CT46GENIChomozygous51407445
103535759135357592T-17GENICheterozygous51407447
103535909035359091T-23GENIChomozygous51407457
103535979235359793T-38GENIChomozygous51407459
103535987935359880AG38GENIChomozygous51407461
103536005435360055AG28GENIChomozygous51407463
103536040035360401TC28GENIChomozygous51407465
103536179435361795CT34GENIChomozygous51407466
103536276435362767TTT---11GENIChomozygous51407468
103536334335363344G-28GENIChomozygous51407472
103536334835363349G-25GENICpossibly homozygous51407476
103536349935363500CT27GENIChomozygous51407478
103536470935364714AGTTT-----37GENIChomozygous51407480
103536603835366039AAAG37GENICpossibly homozygous51407482
103536657735366578AG34GENIChomozygous51407484
103536903935369040TTACACACACACACAC35GENIChomozygous52435317
103536931335369314GA35GENIChomozygous51407486
103536963335369634TTTA28GENIChomozygous51407490
103537226335372264TC16GENIChomozygous51407492
103537262335372624TA39INTERGENIChomozygous51407494