# IntSplice2 prediction with annotation (tab-separated file format)
Column 1: chromosome number
Column 2: position on genome
Column 3: reference nucleotide
Column 4: altered nucleotide
Column 5: start position of affected exon
Column 6: end position of affected exon
Column 7: SNV position form the 3' end of intron
Column 8: strand
Column 9: gene name, Ensembl 101 ID and exon number
Column 10: IntSplice2 prediction (0~1, pathogenic >= 0.5 )