No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1044544 |
chr11:26506962-26967285 |
Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
6 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv916187 |
chr11:26576875-27328603 |
Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
15 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv983164 |
chr11:26743632-26793942 |
Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv1036747 |
chr11:26758984-26781674 |
Enhancers Weak transcription Active TSS Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
5 |
esv2066157 |
chr11:26759726-26759728 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv2608727 |
chr11:26759727-26759728 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
7 |
esv1611573 |
chr11:26759727-26759729 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|