chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094261264094262TC31GENIChomozygous996051205
1264095002264095003TC20GENIChomozygous996051206
1264095472264095473TC18GENIChomozygous996051207
1264095886264095887AG18GENIChomozygous996051208
1264096218264096219CT25GENIChomozygous996051209
1264096731264096732GA26GENIChomozygous996051210
1264097115264097116CT30GENIChomozygous996051211
1264097200264097201GA15GENIChomozygous996051212
1264097208264097209TC15GENIChomozygous996051213
1264097432264097433TC21GENIChomozygous996051214
1264097633264097634AC19GENIChomozygous996051215
1264098036264098037GT33GENIChomozygous996051216
1264098042264098043GA29GENIChomozygous996051217
1264098403264098404TC21GENIChomozygous996051218
1264098424264098425GA22GENIChomozygous996051219
1264099576264099577CT16GENIChomozygous996051220
1264099875264099876CT18GENIChomozygous996051221
1264100059264100060TA19GENIChomozygous996051222
1264100188264100189AG23GENIChomozygous996051223
1264100452264100453CA23GENIChomozygous996051224
1264100637264100638TC29GENIChomozygous996051225
1264100695264100696GA30GENIChomozygous996051226
1264103421264103422CT24GENIChomozygous996051227
1264105400264105401TG25GENIChomozygous996051228
1264105443264105444AC25GENIChomozygous996051229