chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG11GENICpossibly homozygous545928597
10103658439103658440AG14GENIChomozygous545928598
10103658608103658609CT12GENICpossibly homozygous547745693
10103659475103659476AC18GENICheterozygous545928599
10103660927103660928GA14GENIChomozygous547745694
10103661388103661389CG21GENIChomozygous547745695
10103662020103662021CT12GENIChomozygous547745696
10103662594103662595AG9GENIChomozygous547745697
10103663639103663640CT25GENIChomozygous547745698
10103664257103664258CT15GENICpossibly homozygous547745699
10103665617103665618CT21GENIChomozygous547745700
10103665767103665768AG14GENIChomozygous545928600
10103665802103665803CT20GENICpossibly homozygous547745701
10103666999103667000GA11GENICpossibly homozygous547745702
10103667623103667624CT24GENICheterozygous545928601
10103667793103667794AG13GENICheterozygous545928602
10103667854103667855AG17GENICpossibly homozygous545928603
10103668206103668210GTGT----6GENIChomozygous698405761
10103668953103668954CT24GENICpossibly homozygous547745703
10103669968103669969CT14GENIChomozygous545928604
10103670836103670837GA5GENIChomozygous547745704