chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117139845571398456TC11GENICheterozygous50821818
117139951071399511CG13GENIChomozygous50821820
117140477971404780T-14GENICheterozygous50961460
117140498371404984AG12GENICheterozygous50961461
117140632071406321TA8GENIChomozygous50821831
117140761371407614GC9GENIChomozygous50992405
117140942071409421GT8GENIChomozygous50992406
117140947471409475T-9GENIChomozygous50992407
117140947671409477T-9GENIChomozygous50992408
117140987471409875CG19GENIChomozygous50992409
117141559871415599TC13GENICheterozygous50821845
117141821471418215CT18GENICheterozygous50891693
117141872971418730TA14GENICheterozygous50961468