chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101430879714308798GGTT6GENICheterozygous51623018
101430879714308798GGTTTTTT6GENICheterozygous52457988
101430921614309217TG24GENIChomozygous51623019
101431029914310300GA45GENIChomozygous51623020
101431119614311197AG82GENIChomozygous51623021
101431123814311239CT71GENIChomozygous51623022
101431221514312216CCT4GENICheterozygous51329161
101431293414312935GA38GENIChomozygous51623024
101431318414313185AAGTGTGT34GENICpossibly homozygous51623025
101431341414313415TTG32GENIChomozygous51329162
101431393514313936AC42GENIChomozygous51623026
101431419714314198AG42GENIChomozygous51623027
101431420014314201AG41GENIChomozygous51623028
101431632314316324TC42GENIChomozygous51623038
101431645714316458G-59GENIChomozygous51623039
101431718514317186AG31GENIChomozygous51623040
101431741814317419TC17GENIChomozygous51623041
101431742014317421GGGCACCAACACT17GENIChomozygous51623042
101431887014318871GC39GENIChomozygous51623044
101432029314320294CA58GENIChomozygous51623045
101432120914321210TG57GENIChomozygous51623046
101432459114324592AG34GENIChomozygous51623047
101432578414325785TA25GENIChomozygous51623048
101432817314328174A-2GENIChomozygous51329165
101433137214331373GT46GENIChomozygous51623049
101433152014331521TA50GENIChomozygous51623050
101431208914312090AATTTTTTTT3GENIChomozygous52481393
101431420714314219TGATGATGTTGT------------21GENIChomozygous52481395
101431508914315203GGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTGTAGCCC------------------------------------------------------------------------------------------------------------------57GENICpossibly homozygous52313057