No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1048356 |
chr11:100713096-101058995 |
Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
8 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv541154 |
chr11:100713096-101058995 |
Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
8 gene(s)
|
inside rSNPs
|
diseases
|
3 |
esv2762939 |
chr11:100908670-100913694 |
Weak transcription Enhancers Strong transcription Genic enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
4 |
nsv556130 |
chr11:100909186-100912736 |
Weak transcription Genic enhancers Enhancers Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|