Enter the SNP position(s), such as 14267556 14267914 (for chr10)The number of bases on the left and right (default: 500 bp)
OR give a range, like 14266556 - 14268968 (for chr10)
The cutoff (default=0.25) of the minor allele (the second most abundant) frequency
Spread around SNPs?YesNo
Number of errors in motif search (default: 1)?
You can search any motif (format: A[CT].GC)