chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141705444141705445TC10GENIChomozygous54159553
7141705520141705521TC20GENIChomozygous54159554
7141706317141706318TTC3GENIChomozygous54159555
7141706353141706354C-4GENIChomozygous54159556
7141707577141707578CA34GENIChomozygous54159558
7141707812141707813CCAGAG25GENIChomozygous54159559
7141709047141709048AG23GENIChomozygous54159560
7141709856141709857AG38GENIChomozygous54159561
7141710147141710148CCA16GENICpossibly homozygous54159562
7141710627141710628AAT8GENICpossibly homozygous54159563
7141710738141710739T-4GENIChomozygous54159565
7141711200141711201CCT6GENICheterozygous54159566
7141711217141711220TTC---15GENICheterozygous55017214
7141712736141712737CCAGTGCCTCCAT19GENIChomozygous54159567
7141715671141715672TTATTA4GENIChomozygous54159570
7141717110141717111GGTT16GENIChomozygous54159571