chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5104328387104328388TC13GENIChomozygous565616113
5104328650104328651GA34GENIChomozygous565616114
5104328758104328759AAATACATACATACATACATAC9GENIChomozygous710076175
5104329030104329032TT--3GENIChomozygous710076176
5104331078104331080TT--7GENICpossibly homozygous710076177
5104331756104331757C-27GENIChomozygous710076179
5104332402104332403AATGTG17GENICheterozygous710076182
5104332402104332403AATGTGTG17GENICpossibly homozygous710076183
5104332877104332878GC15GENIChomozygous565616115
5104333978104333979AG10GENIChomozygous565616116
5104335541104335542AG16GENIChomozygous565616117