chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125044761050447611CG15GENIChomozygous115352303
125044785450447855AC14GENIChomozygous115352305
125044820350448204CT14GENIChomozygous115352307
125044888750448888GA20GENIChomozygous115352309
125044946450449465GA21GENIChomozygous115352312
125044957250449573AT19GENIChomozygous115352314
125044959550449596TG20GENIChomozygous115352316
125044966050449661TC19GENIChomozygous115403598
125044970850449709TC8GENICheterozygous115506205
125044978250449783CA16GENIChomozygous115352318
125045000250450003GA13GENIChomozygous115352320
125045047450450475GT14GENIChomozygous115352322
125045413450454135TC20GENIChomozygous115352328
125045420150454202GA41GENIChomozygous115352330
125045508450455085CT22GENIChomozygous115352332
125045662050456621TG29GENIChomozygous115352334
125045747650457477AG18GENIChomozygous115352336
125045787750457878AG28GENIChomozygous115352338
125045825850458259AG28GENIChomozygous115352340
125046097450460975GA22GENIChomozygous115352342