chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2270330560270330562TT--1GENIChomozygous59570113
2270330564270330565CCG1GENIChomozygous59570114
2270333426270333427T-17GENIChomozygous59570117
2270333741270333742GA19GENIChomozygous59570118
2270333781270333782TA16GENIChomozygous59570119
2270334079270334080AC25GENIChomozygous59570120
2270334198270334199CA27GENIChomozygous59570121
2270334816270334817TC16GENIChomozygous59570122
2270335131270335137TGCTAT------15GENIChomozygous59570123
2270335948270335949GC26GENIChomozygous59570124
2270336382270336383CG13GENICpossibly homozygous59570125
2270337210270337211AG29GENIChomozygous59570127
2270338247270338248AG22GENIChomozygous59570128
2270338294270338295GA20GENIChomozygous59570129
2270338507270338508TTA22GENIChomozygous59570130
2270338706270338707AT20GENIChomozygous59570131
2270339043270339044GA24GENIChomozygous59570132
2270339313270339314TC23GENIChomozygous59570133
2270339342270339343AC22GENIChomozygous59570134
2270336383270336384CCAAAAA13GENICheterozygous60530568
2270336383270336384CCAAAAAAAA13GENICpossibly homozygous60530569