Perturb Site Without Side Effects

Often researchers want to assess functionality of a TF binding site by ablating the site, or assess the role on affinity by optimizing or reducing the affinity of the site. It is important to ensure that the chosen mutation does not have any unintended sidefects. For example, a mutation that ablates your site of interest could also create a binding site that didn’t exist in the original sequence.

The Perturb Site Without Side Effects Module enumerates all mutations that either ablate, optimize affinity or reduce affinity the site. For each mutation, it reports any secondary effects on other TF binding sites the mutation has. The best mutation is one that has the intended effect (ablation or optimization) with minimal side effects.

This module can also be used to ensure PAM deletions for CRISPR experiments do not alter existing binding sites.

Links: Tutorial Video Documentation

Enter Enhancer DNA sequence

DNA Sequence to Annotate
*30-bp DNA sequence to annotate. Only use upper case A/T/C/G.
What do you want to perturb?


Specify one or more mutation types to analyze. The possible mutation types affinity optimizations, affinity reduction, creation of de novo site, and site ablation. By default all of the listed mutation types are analyzed.

Only SNVs with a fold change above this threshold will be reported. By default, all SNVs will be reported.

Only SNVs with a fold change below this threshold will be reported. By default all SNVs will be reported.

TF Family*
Select TF family.
TF PBM Dataset*
Select TF PBM dataset.
Core Site*
IUPAC formatted core binding site.
Affinity Normalization*
Select normalization method.

Search for and select JASPAR motifs to analyze (e.g. type "ETS" to find Ets1)
Selected motif, it filters:
Minimum score for PWM to predict a site. Default is 0.8.
Enter the PAM sequence to analyze.
What Secondary Effects do you want to consider?