chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2270330560270330562TT--6GENIChomozygous59570113
2270330564270330565CCG6GENIChomozygous59570114
2270333145270333146GA9GENIChomozygous59570115
2270333426270333427T-22GENIChomozygous59570117
2270333741270333742GA24GENICpossibly homozygous59570118
2270333781270333782TA19GENICheterozygous59570119
2270334079270334080AC23GENIChomozygous59570120
2270334198270334199CA20GENIChomozygous59570121
2270334816270334817TC16GENIChomozygous59570122
2270335948270335949GC18GENIChomozygous59570124
2270336382270336383CG12GENICheterozygous59570125
2270336383270336384CCAA6GENIChomozygous59570126
2270337210270337211AG37GENIChomozygous59570127
2270338247270338248AG15GENIChomozygous59570128
2270338294270338295GA21GENIChomozygous59570129
2270338507270338508TTA17GENIChomozygous59570130
2270338706270338707AT28GENIChomozygous59570131
2270339342270339343AC15GENIChomozygous59570134
2270336357270336358CA21GENICheterozygous59978831
2270337154270337155GA37GENIChomozygous59978832
2270337174270337175GA36GENIChomozygous59978833
2270339648270339649AT25GENIChomozygous59978834
2270339850270339851CT20GENIChomozygous59978835