chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178467601178467602AG19GENIChomozygous108403887
1178467849178467850GT17GENIChomozygous109525296
1178468164178468165AG16GENIChomozygous108403889
1178468222178468223CT6GENIChomozygous109525297
1178468674178468675GT11GENIChomozygous109525298
1178468752178468753GA16GENIChomozygous109525299
1178469111178469112CG15GENIChomozygous108403891
1178469128178469129CT15GENIChomozygous109525300
1178469200178469201CT22GENIChomozygous109525301
1178469807178469808TC10GENIChomozygous109525302
1178469904178469905AG16GENIChomozygous109525303
1178470191178470192GA23GENIChomozygous120781571
1178470193178470194AG22GENIChomozygous120781572
1178470568178470569TC26GENIChomozygous109525304
1178470727178470728CT20GENIChomozygous109525305
1178471279178471280GA17GENIChomozygous109525306
1178471371178471372AG25GENIChomozygous109525307
1178471808178471809TC18GENIChomozygous109525308
1178471952178471953TC22GENIChomozygous109525309
1178472330178472331CT33GENIChomozygous109525310
1178472452178472453TA25GENIChomozygous109525311
1178472674178472675CT14GENIChomozygous109525312
1178472681178472682TC18GENIChomozygous109525313
1178472759178472760TG19GENIChomozygous109525314
1178473008178473009AG11GENIChomozygous109525315
1178473439178473440GA26GENIChomozygous109525316
1178473467178473468TC30GENIChomozygous109525317
1178473510178473511GA29GENIChomozygous109525318
1178473851178473852TC31GENIChomozygous109525319
1178474879178474880CT13GENIChomozygous109525323
1178475027178475028CT15GENIChomozygous109525324