chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101430857714308578AAT3GENICheterozygous51623016
101430857814308581TTT---3GENICheterozygous51623017
101430879714308798GGTT37GENIChomozygous51623018
101430921614309217TG49GENIChomozygous51623019
101431029914310300GA50GENIChomozygous51623020
101431119614311197AG70GENICpossibly homozygous51623021
101431123814311239CT69GENICpossibly homozygous51623022
101431208914312090AATTTTTT9GENIChomozygous51623023
101431221514312216CCT4GENICheterozygous51329161
101431293414312935GA58GENICpossibly homozygous51623024
101431318414313185AAGTGTGT20GENIChomozygous51623025
101431341414313415TTG70GENIChomozygous51329162
101431393514313936AC41GENIChomozygous51623026
101431419714314198AG37GENICheterozygous51623027
101431420014314201AG36GENICheterozygous51623028
101431420314314204AG34GENICheterozygous51623029
101431420914314210AG23GENICpossibly homozygous51623030
101431421214314213AG23GENICpossibly homozygous51623031
101431421514314216TG26GENICpossibly homozygous51623032
101431421814314219TA26GENICpossibly homozygous51623033
101431512014315121AG8GENIChomozygous51623034
101431512614315127AC7GENIChomozygous51623035
101431519614315197GA29GENICheterozygous51623036
101431520214315203CA31GENICheterozygous51623037
101431632314316324TC46GENIChomozygous51623038
101431645714316458G-47GENIChomozygous51623039
101431718514317186AG60GENICpossibly homozygous51623040
101431741814317419TC26GENIChomozygous51623041
101431742014317421GGGCACCAACACT28GENIChomozygous51623042
101431777214317773AG31GENICpossibly homozygous51623043
101431777314317774AG32GENICpossibly homozygous51329163
101431887014318871GC45GENIChomozygous51623044
101431968614319687C-38GENICheterozygous51329164
101432029314320294CA62GENIChomozygous51623045
101432120914321210TG55GENIChomozygous51623046
101432459114324592AG57GENIChomozygous51623047
101432578414325785TA45GENIChomozygous51623048
101432817314328174A-23GENICheterozygous51329165
101433137214331373GT50GENIChomozygous51623049
101433152014331521TA46GENIChomozygous51623050