No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv873634 |
chr2:10275814-10337034 |
Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionmiRNA
|
11 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv873635 |
chr2:10286466-10344465 |
Weak transcription Bivalent Enhancer Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
9 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv873636 |
chr2:10300390-10331919 |
Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS
|
Chromatin interactive region
|
7 gene(s)
|
inside rSNPs
|
diseases
|
4 |
esv3340132 |
chr2:10328101-10332799 |
Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer
|
TF binding regionChromatin interactive regionmiRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
5 |
esv3372133 |
chr2:10328701-10332599 |
Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|