chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141705444141705445TC13GENIChomozygous54159553
7141705520141705521TC28GENIChomozygous54159554
7141706317141706318TTC9GENIChomozygous54159555
7141706353141706354C-7GENICpossibly homozygous54159556
7141707415141707416TTCCCC3GENICheterozygous54267492
7141707415141707416TTCCC3GENICheterozygous54267495
7141707577141707578CA15GENIChomozygous54159558
7141707812141707813CCAGAG21GENIChomozygous54159559
7141709047141709048AG37GENIChomozygous54159560
7141709856141709857AG24GENIChomozygous54159561
7141710147141710148CCA17GENICheterozygous54159562
7141710627141710628AAT7GENICpossibly homozygous54159563
7141710738141710739T-8GENIChomozygous54159565
7141711200141711201CCT6GENICheterozygous54159566
7141712736141712737CCAGTGCCTCCAT35GENIChomozygous54159567
7141715671141715672TTATTA8GENIChomozygous54159570
7141717110141717111GGTT26GENIChomozygous54159571