To make the EGFRvIII mutant cell line in H9, gene editing was performed using CRISRP-CAS9 with two sgRNAs. This is the sequencing data for EGFR site for mutant cell line. Off-target position of each s
Mouse embryonic stem cells (i.e., mESCs; line ESC 129-B13) were genetically modified using CRISPR-Cas9 to mutate the H3f3b locus, in order to carry homozygous lysine-to-alanine substitution of residue
