No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv948878 |
chr2:213345197-213534298 |
Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
2 |
esv3459104 |
chr2:213465833-213470603 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
3 |
esv3459102 |
chr2:213465857-213470603 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
4 |
esv3459103 |
chr2:213465897-213470559 |
Weak transcription Enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
5 |
esv3459105 |
chr2:213465897-213470559 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
6 |
nsv524959 |
chr2:213468813-213472634 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
7 |
esv3692759 |
chr2:213468813-213473115 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|