No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv916392 |
chr8:50827638-51395140 |
Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv948436 |
chr8:51115028-51917504 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv6185 |
chr8:51213648-51237196 |
Enhancers Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
4 |
esv1828291 |
chr8:51225111-51246823 |
ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
5 |
esv1832233 |
chr8:51225111-51256438 |
ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv1827302 |
chr8:51225496-51246823 |
Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
7 |
esv1190798 |
chr8:51236414-51236421 |
Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|