| 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 |
esv1848303 |
chr12:40867011-40887238 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv1850439 |
chr12:40867211-40887867 |
Enhancers ZNF genes & repeats Weak transcription Strong transcription
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv20428 |
chr12:40867874-40884927 |
Weak transcription Enhancers ZNF genes & repeats Strong transcription
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3390786 |
chr12:40871685-40877783 |
ZNF genes & repeats Weak transcription Strong transcription
|
lncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3500652 |
chr12:40872785-40877883 |
Weak transcription ZNF genes & repeats Strong transcription
|
lncRNA
|
n/a
|
inside rSNPs
|
diseases
|
