ABSOLUTE input maf file problem

I'm trying to run ABSOLUTE v1.0.6, but it appeared error with maf file downloaded on TCGA.
I have checked the colume, it seems no problem. This is error:
=======================================================================
Error: bad restore file magic number (file may be corrupted) -- no data loaded
In addition: Warning message:
file ‘TCGA.BRCA.mutect.9408fdf2-013f-4c09-8821-a709af56b9ff.somatic.maf’ has magic number 'Hugo_'
Use of save versions prior to 2 is deprecated.
=======================================================================

I tryed make chrom column to be the first column(as ABSOLUTE said the specific information of
input file), nothing changed but ''Chrom":

=======================================================================
Error: bad restore file magic number (file may be corrupted) -- no data loaded
In addition: Warning message:
file ‘TCGA-3C-AAAU-01A-11D-A41F-09.maf’ has magic number 'Chrom'
Use of save versions prior to 2 is deprecated
=======================================================================

It seems nothing loaded. why appeared this problem? Although I use the original maf file downloaded on TCGA, it also appeared the same error.

This is the header of my maf file(from TCGA):

Hugo_Symbol Entrez_Gene_Id Center NCBI_Build Chromosome Start_Position End_Position Strand Variant_Classification Variant_Type Reference_Allele Tumor_Seq_Allele1 Tumor_Seq_Allele2 dbSNP_RS dbSNP_Val_Status Tumor_Sample_Barcode Matched_Norm_Sample_Barcode Match_Norm_Seq_Allele1 Match_Norm_Seq_Allele2 Tumor_Validation_Allele1 Tumor_Validation_Allele2 Match_Norm_Validation_Allele1 Match_Norm_Validation_Allele2 Verification_Status Validation_Status Mutation_Status Sequencing_Phase Sequence_Source Validation_Method Score BAM_File Sequencer Tumor_Sample_UUID Matched_Norm_Sample_UUID HGVSc HGVSp HGVSp_Short Transcript_ID Exon_Number t_depth t_ref_count t_alt_count n_depth n_ref_count n_alt_count all_effects Allele Gene Feature Feature_type Consequence cDNA_position CDS_position Protein_position Amino_acids Codons Existing_variation ALLELE_NUM DISTANCE TRANSCRIPT_STRAND SYMBOL SYMBOL_SOURCE HGNC_ID BIOTYPE CANONICAL CCDS ENSP SWISSPROT TREMBL UNIPARC RefSeq SIFT PolyPhen EXON INTRON DOMAINS GMAF AFR_MAF AMR_MAF ASN_MAF EAS_MAF EUR_MAF SAS_MAF AA_MAF EA_MAF CLIN_SIG SOMATIC PUBMED MOTIF_NAME MOTIF_POS HIGH_INF_POS MOTIF_SCORE_CHANGE IMPACT PICK VARIANT_CLASS TSL HGVS_OFFSET PHENO MINIMISED ExAC_AF ExAC_AF_AFR ExAC_AF_AMR ExAC_AF_EAS ExAC_AF_FIN ExAC_AF_NFE ExAC_AF_OTH ExAC_AF_SAS GENE_PHENO FILTER src_vcf_id tumor_bam_uuid normal_bam_uuid GDC_Validation_Status GDC_Valid_Somatic

I don't know where is the problem located, so I have no idea to solve the problem.

Sincerely thanks for your help

Cisplain