No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv869116 |
chr4:175231090-175801761 |
Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
13 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv1018390 |
chr4:175475505-175969742 |
Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
12 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv880584 |
chr4:175505749-175644689 |
Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
4 |
esv988593 |
chr4:175620441-175627158 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
5 |
nsv596235 |
chr4:175621502-175626769 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv3466671 |
chr4:175623177-175628675 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
7 |
esv3359677 |
chr4:175623727-175628225 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
8 |
esv2038865 |
chr4:175623731-175623732 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|