chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226976491226976492CT23GENICpossibly homozygous121187054
1226977111226977119TCTGTGTG12GENIChomozygous135288216
1226985506226985507AT18GENIChomozygous121187057
1226985571226985573CA13GENIChomozygous135288217
1226987423226987424AG28GENICpossibly homozygous108998593
1226985919226985921TT15GENICheterozygous131992469
1226985922226985932ATTCATTCAT15GENICheterozygous131992470