chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176773548176773549AC14GENICpossibly homozygous55849657
5176773674176773675TC11GENIChomozygous56101458
5176773706176773707GA10GENIChomozygous56101460
5176774156176774157TC11GENICpossibly homozygous56101462
5176774877176774878CT14GENICheterozygous56101464
5176776162176776163GA7GENIChomozygous56101466
5176776749176776750GC12GENIChomozygous56101468
5176777787176777788CT11GENICpossibly homozygous56101470
5176780126176780127GA5GENIChomozygous56101472
5176781354176781355CG17GENIChomozygous56101474
5176781467176781468TC13GENICpossibly homozygous56101476