chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124339161124339162GC31GENIChomozygous955431636
7124339853124339854CT29GENIChomozygous955431637
7124340150124340151TC26GENIChomozygous955431638
7124341609124341610CA24GENICpossibly homozygous955431639
7124344290124344291CA32GENIChomozygous955431640
7124344725124344726AG19GENIChomozygous955431641
7124346017124346018AG26GENIChomozygous955431642
7124351259124351260TG28GENIChomozygous955431643
7124351260124351261GC28GENIChomozygous955431644
7124351265124351266AG22GENIChomozygous955431645
7124354543124354544TC31GENIChomozygous955431646
7124356107124356108GA19GENIChomozygous955431647
7124357590124357591CT21GENIChomozygous955431648
7124360113124360114CT14GENIChomozygous955431649
7124361076124361077AG26GENIChomozygous955431650
7124361238124361239CT25GENIChomozygous955431651
7124361846124361847GA37GENIChomozygous955431652
7124366145124366146TC29GENIChomozygous955431653