chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2215520288215520289TTGTTGTGTATG21GENIChomozygous60457346
2215520339215520340GGCTTTGTATGGTTGTGTATGGCTGTGTATGGCTGTGTATGA5GENIChomozygous60516702
2215520357215520358AATGGCTGTG2GENIChomozygous60516703
2215521832215521833A-16GENICpossibly homozygous59391114
2215521978215521979AAT36GENIChomozygous59391115
2215522124215522125CA46GENIChomozygous59391116
2215522131215522132CT49GENIChomozygous59391117
2215522890215522891GA54GENIChomozygous59391118
2215524758215524760AA--31GENIChomozygous59391119
2215524819215524820CCTGTTTGTT24GENIChomozygous59391120
2215525125215525126GA30GENIChomozygous59391122
2215525501215525502GGA26GENICheterozygous59391123
2215525502215525503A-26GENICheterozygous59773682
2215526203215526204CT19GENIChomozygous59391124
2215526294215526295AG28GENIChomozygous59391125
2215526993215526997TTAG----32GENIChomozygous59391126
2215527530215527531C-26GENIChomozygous59391127
2215527812215527813GGA3GENIChomozygous59391128
2215527824215527825CCAAAAAAAAAAA7GENIChomozygous60516704
2215528000215528001TC38GENIChomozygous59391130
2215528722215528723GGA34GENIChomozygous59391131
2215529010215529011GT34GENIChomozygous59391132
2215532699215532700TA41GENIChomozygous59391133
2215534009215534011TA--28GENIChomozygous59391134
2215534041215534042GA37GENIChomozygous59391135
2215534660215534661AAT21GENICpossibly homozygous59391136