chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2215520094215520095CT54GENICheterozygous59391098
2215520122215520123GT64GENICheterozygous59391099
2215520124215520125TC61GENICheterozygous59391100
2215520143215520144GA68GENICheterozygous59391101
2215520177215520178CT44GENICheterozygous59391102
2215520187215520188TC44GENICheterozygous59391103
2215520211215520212AG32GENIChomozygous59391104
2215520239215520240TG38GENICheterozygous59391105
2215520255215520256GT43GENICheterozygous59391106
2215520310215520311CT35GENICheterozygous59391107
2215520320215520321TC34GENICheterozygous59391108
2215520340215520341TC30GENICheterozygous59391109
2215520357215520358AG25GENICheterozygous59391110
2215520372215520375GTT---24GENICheterozygous59391111
2215520396215520397TC28GENICheterozygous59391112
2215520397215520407TGTGTATGGC----------10GENICheterozygous59391113
2215521832215521833A-1GENIChomozygous59391114
2215521978215521979AAT35GENIChomozygous59391115
2215522124215522125CA49GENIChomozygous59391116
2215522131215522132CT49GENIChomozygous59391117
2215522890215522891GA65GENIChomozygous59391118
2215524758215524760AA--34GENIChomozygous59391119
2215524819215524820CCTGTTTGTT17GENICpossibly homozygous59391120
2215524819215524820CCTGTTTGTTTGTT17GENICheterozygous59391121
2215525125215525126GA44GENIChomozygous59391122
2215525501215525502GGA18GENICheterozygous59391123
2215526203215526204CT22GENIChomozygous59391124
2215526294215526295AG46GENICpossibly homozygous59391125
2215526993215526997TTAG----33GENIChomozygous59391126
2215527530215527531C-28GENIChomozygous59391127
2215527812215527813GGA5GENIChomozygous59391128
2215527823215527825CC--15GENICheterozygous59391129
2215528000215528001TC48GENIChomozygous59391130
2215528722215528723GGA36GENIChomozygous59391131
2215529010215529011GT36GENIChomozygous59391132
2215532699215532700TA47GENIChomozygous59391133
2215534009215534011TA--32GENIChomozygous59391134
2215534041215534042GA42GENIChomozygous59391135
2215534660215534661AAT16GENICpossibly homozygous59391136