chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103533478835334789CT22GENIChomozygous52302181
103533546035335461CCAGCTACAGCGTACTTATATATAATAAATGAATAAATCTTTAAAAAAAAA11GENIChomozygous52367390
103533621235336213CA13GENIChomozygous52137669
103533720135337202GGT8GENIChomozygous51407432
103535288635352887GGAC15GENICheterozygous51407437
103535288635352887GGACACAGACAC15GENICheterozygous52647434
103535296935352970AAT12GENIChomozygous51407443
103535638735356388CCAAAAAAAAAAAAAAAA5GENIChomozygous52367392
103535663535356636CT17GENIChomozygous52302183
103535909035359091T-17GENIChomozygous51407457
103535979235359793T-24GENIChomozygous51407459
103535987935359880AG22GENIChomozygous51407461
103536005435360055AG24GENIChomozygous51407463
103536040035360401TC16GENIChomozygous51407465
103536179435361795CT29GENIChomozygous51407466
103536276435362767TTT---12GENICheterozygous51407468
103536276535362767TT--12GENICheterozygous51407470
103536334335363344G-20GENIChomozygous51407472
103536334535363349TTTG----20GENIChomozygous52367394
103536349935363500CT22GENIChomozygous51407478
103536603835366039AAAG17GENICpossibly homozygous51407482
103536657735366578AG20GENIChomozygous51407484
103536890635368907GA10GENIChomozygous52302185
103536904035369044ACAC----14GENIChomozygous52302187
103536963235369633GGTT26GENIChomozygous51407488
103536964035369641GGT20GENICpossibly homozygous51846468
103537380435373805TG31INTERGENIChomozygous52302189
103537549335375494GA11INTERGENIChomozygous52302191