chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141705444141705445TC13GENIChomozygous54159553
7141705520141705521TC29GENIChomozygous54159554
7141706317141706318TTC10GENIChomozygous54159555
7141706353141706354C-5GENIChomozygous54159556
7141707415141707416TTCCCC5GENICheterozygous54267492
7141707415141707416TTCCC5GENICheterozygous54267495
7141707577141707578CA20GENIChomozygous54159558
7141707812141707813CCAGAG26GENIChomozygous54159559
7141709856141709857AG26GENIChomozygous54159561
7141710147141710148CCA12GENICpossibly homozygous54159562
7141710627141710628AAT6GENIChomozygous54159563
7141710738141710739T-2GENIChomozygous54159565
7141711200141711201CCT10GENICpossibly homozygous54159566
7141712736141712737CCAGTGCCTCCAT28GENIChomozygous54159567
7141715671141715672TTATTA2GENIChomozygous54159570
7141717110141717111GGTT16GENIChomozygous54159571