No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv882727 |
chr5:113548400-113602162 |
Weak transcription Enhancers Flanking Active TSS Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv1029021 |
chr5:113551892-113599644 |
Enhancers Weak transcription Flanking Active TSS Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv537865 |
chr5:113551892-113599644 |
Enhancers Weak transcription Active TSS Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv1024203 |
chr5:113596392-113659935 |
Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
5 |
nsv965570 |
chr5:113596430-113622354 |
Enhancers Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
6 |
nsv1021335 |
chr5:113599444-113659146 |
Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
7 |
nsv537866 |
chr5:113599444-113659146 |
Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|