chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204641481446414815TG67INTERGENICheterozygous63651968
204641481846414819TC83INTERGENICheterozygous63517106
204641482046414821CG92INTERGENICheterozygous63651969
204641484446414845CT119INTERGENICheterozygous63651970
204641486746414868AG134INTERGENICheterozygous63651971
204641806046418061CA32INTERGENIChomozygous63517108
204642204746422048TG35INTERGENICpossibly homozygous63517109
204642205346422054CG31INTERGENIChomozygous63517110
204642206446422065TG30INTERGENIChomozygous63517111
204642791846427919CA34INTERGENIChomozygous63517113
204642794246427943GT43INTERGENIChomozygous63517114
204642798246427983CT52INTERGENIChomozygous63517115
204643546646435467TC17INTERGENIChomozygous63517130
204643546846435469GA16INTERGENIChomozygous63517131
204643547046435471TA16INTERGENIChomozygous63517132
204643548246435483TG26INTERGENIChomozygous63517133
204643549746435498GC30INTERGENIChomozygous63517134
204643550146435502CT28INTERGENIChomozygous63517135
204643551346435514GC35INTERGENIChomozygous63517136
204643551946435520TC31INTERGENIChomozygous63517137
204643552546435526TA31INTERGENIChomozygous63517138
204643553146435532TC35INTERGENIChomozygous63517139
204643554446435545TA37INTERGENIChomozygous63517140
204643555746435558TA37INTERGENIChomozygous63517141
204643556146435562TA38INTERGENIChomozygous63517142