| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv898362 |
chr11:106715879-106809457 |
ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
nsv1036990 |
chr11:106718613-106774766 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv541162 |
chr11:106718613-106774766 |
Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv556231 |
chr11:106737224-106815963 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv474 |
chr11:106757020-106795146 |
ZNF genes & repeats Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv531938 |
chr11:106760733-107156814 |
Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
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Last update: Aug 31, 2015