Use of ePOSSUM is easy: simply enter the DNA variant you want to
analyse into the
variant or genomic region (build 37) field.
This allows the software to find known TF binding sites at this
position - as we rely on the ENCODE data we can only use genome
version 37 for this.
If you do not know the location but have
a wild-type and a variant sequence, you can still enter them into the
sequence(s) to test fields. In this case, we cannot display any
known TF binding sites.
We provide a detailed
documentation of ePOSSUM's
output.
Please note that ePOSSUM only works with
human TFs.