No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv899033 |
chr12:40758652-41122288 |
Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
23 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv518952 |
chr12:40857620-40867333 |
Enhancers Weak transcription
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
3 |
esv2476758 |
chr12:40864242-40865712 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
4 |
esv2048308 |
chr12:40864827-40865263 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
5 |
esv3496898 |
chr12:40864834-40865217 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv3496900 |
chr12:40864858-40865197 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
7 |
esv3496899 |
chr12:40864878-40865170 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
8 |
esv3486008 |
chr12:40864905-40865133 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
9 |
esv3496896 |
chr12:40864912-40865142 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
10 |
esv3445636 |
chr12:40864932-40865112 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|