chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2113582706113582707GA27GENIChomozygous59027035
2113583504113583505AACTAAAC24GENIChomozygous59027036
2113583924113583925AT34GENIChomozygous59027037
2113584093113584094TC20GENIChomozygous59027038
2113584290113584291AG23GENIChomozygous59846063
2113585942113585943CT20GENIChomozygous59027039
2113586045113586046GT33GENIChomozygous59027040
2113586111113586112TC20GENICpossibly homozygous59027041
2113586192113586193AAG31GENIChomozygous59027042
2113586194113586195AAGC32GENIChomozygous59027043
2113586348113586349CCTGAG33GENIChomozygous59027044