Putative TFBSs overlaying detected SNPs#.

#For a complete list of identified TFBS coinciding with detected SNPs see supplementary table S1.alocation of the SNP/TFBS with respect to the RPS19 open reading frame.bdatabase identifier (dbSNP) for previously described SNPs or number of novel SNP, respectively.cSNP alleles, indicating reference and alternative (replace) allele.dname of transcription factor or motif recognized, as named in the databases.elibrary, version of the library and identifier to which a TFBS is associated under a PWM database release.fmotif recognized (5�� to 3�� sequence). Allele positioning marked in bold. Alleles falling exactly adjacent to the end of a motif highlighted in bold and italics. Capital letters highlight important positions for the putative binding strength of a motif. Chromosome, start, end position and strand within the human reference genome (hg18, build 36.1).gscore for the reference genome allele. MATCH and pMATCH use 1.000 as maximum score between an optimal binding site match and matrix power of detection. TOUCAN detection tools (MotifScanner, MotifLocator, MotifSampler) do not use global maximum or matrix scoring, but the higher the numbers, the better the predicted site. The apriori probability or threshold is stated under the score when any of the TOUCAN tools has been used.hscore for non-reference allele.iprogram used for detection of a motif. Error minimization criteria stated when applicable.jtranscript factor contained in any of the multi-conserved sequence (MCS) region of the multi-species alignment. The first value belongs to the Infocon program and the second to the EPO EnsEMBL track. ��Y�� indicates that the TFBS motif is totally contained in the area (see supplementary figure S1 and file S2), ��y+�� that there is major overlapping part (>75%), ��y�� that there is significant overlapping part (50%), ��y?�� only if a minor part overlaps (