chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2215520288215520289TTGTTGTGTATG18GENIChomozygous60457346
2215520339215520340GGCTTTGTATGGTTGTGTATGGCTGTGTATGGCTGTGTATGA4GENIChomozygous60516702
2215521832215521833A-11GENIChomozygous59391114
2215521978215521979AAT14GENIChomozygous59391115
2215522124215522125CA33GENIChomozygous59391116
2215522131215522132CT35GENIChomozygous59391117
2215522890215522891GA26GENIChomozygous59391118
2215524758215524760AA--21GENIChomozygous59391119
2215524819215524820CCTGTTTGTT26GENIChomozygous59391120
2215525125215525126GA32GENIChomozygous59391122
2215525501215525502GGA13GENIChomozygous59391123
2215526203215526204CT12GENIChomozygous59391124
2215526294215526295AG14GENIChomozygous59391125
2215526993215526997TTAG----18GENIChomozygous59391126
2215527530215527531C-22GENIChomozygous59391127
2215527812215527813GGA3GENIChomozygous59391128
2215527824215527825CCAAAAAAAAAAA1GENIChomozygous60516704
2215528000215528001TC31GENIChomozygous59391130
2215532699215532700TA21GENIChomozygous59391133
2215528722215528723GGA18GENIChomozygous59391131
2215529010215529011GT20GENIChomozygous59391132
2215534009215534011TA--14GENICheterozygous59391134
2215534041215534042GA22GENIChomozygous59391135
2215534660215534661AAT15GENICpossibly homozygous59391136