| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv539555 |
chr8:39683857-40673606 |
Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
26 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv508505 |
chr8:39730094-39791331 |
Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv1033371 |
chr8:39749437-39899540 |
Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
7 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv6165 |
chr8:39765054-39765794 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv2632441 |
chr8:39765076-39766616 |
Weak transcription Strong transcription
|
TF binding region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
esv2072361 |
chr8:39765132-39765842 |
Weak transcription Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3479134 |
chr8:39765198-39765739 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3488337 |
chr8:39765215-39765775 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3488339 |
chr8:39765220-39765774 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3488336 |
chr8:39765244-39765679 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
