Tool for Investigating Allele Specific Binding & Transcription

Enter the chromosome, such as chr10

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?

Number of errors in motif search (default: 1)?

You can search any motif (format: A[CT].GC)

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