chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2215520288215520289TTGTTGTGTATG25GENIChomozygous60457346
2215520339215520340GGCTTTGTATGGTTGTGTATGGCTGTGTATGGCTGTGTATGA8GENIChomozygous60516702
2215520357215520358AATGGCTGTG6GENIChomozygous60516703
2215521832215521833A-11GENICpossibly homozygous59391114
2215521978215521979AAT13GENIChomozygous59391115
2215522124215522125CA27GENIChomozygous59391116
2215522131215522132CT26GENIChomozygous59391117
2215522890215522891GA23GENIChomozygous59391118
2215524758215524760AA--28GENIChomozygous59391119
2215524819215524820CCTGTTTGTTTGTT13GENIChomozygous59391121
2215525125215525126GA22GENIChomozygous59391122
2215525501215525502GGA10GENICpossibly homozygous59391123
2215526203215526204CT21GENICpossibly homozygous59391124
2215526294215526295AG25GENIChomozygous59391125
2215526993215526997TTAG----26GENIChomozygous59391126
2215527530215527531C-25GENIChomozygous59391127
2215527812215527813GGA6GENIChomozygous59391128
2215527824215527825CCAAAAAAAAAAA4GENIChomozygous60516704
2215528000215528001TC20GENIChomozygous59391130
2215528722215528723GGA8GENIChomozygous59391131
2215529010215529011GT25GENIChomozygous59391132
2215532699215532700TA37GENIChomozygous59391133
2215534009215534011TA--16GENICpossibly homozygous59391134
2215534041215534042GA25GENIChomozygous59391135
2215534660215534661AAT14GENICheterozygous59391136