chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116682430266824303CA21GENIChomozygous116247279
116682498966824990AT29GENICpossibly homozygous116247281
116682737066827371CT22GENIChomozygous116247282
116682762266827623CT19GENIChomozygous116247284
116682790466827905GT23GENIChomozygous115888318
116682884466828845TA13GENIChomozygous115888320
116683575866835759TA25GENIChomozygous115888322
116683576166835762TG25GENIChomozygous116247290
116683605566836056CT41GENIChomozygous116048022
116683958166839582AC26GENIChomozygous115888324
116684582566845826CG16GENIChomozygous116247292
116684900666849007TG19GENIChomozygous116247294
116684987666849877TA6GENIChomozygous116247296
116685216566852166CT19GENIChomozygous115888336
116685243066852431GA26GENIChomozygous115888338
116685907866859079TG25GENIChomozygous116247298
116686263066862631CT18GENIChomozygous115888346
116686362866863629GA17GENIChomozygous115888348
116686535266865353TA25GENIChomozygous115888350
116686673366866734CT18GENIChomozygous116247300
116687060766870608CT25GENIChomozygous116247302
116687269966872700TC26GENIChomozygous116105074
116687366066873661GT18GENIChomozygous116105075
116687439566874396CT17GENIChomozygous116247304
116687456966874570CG16GENIChomozygous116247306
116687724266877243CA27GENIChomozygous116247308
116687841566878416CT17GENIChomozygous116247310