| 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 |
nsv556231 |
chr11:106737224-106815963 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv474 |
chr11:106757020-106795146 |
ZNF genes & repeats Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
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
|
| 5 |
esv3466197 |
chr11:106784242-106789940 |
Weak transcription ZNF genes & repeats Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv1819607 |
chr11:106784955-106789492 |
Enhancers Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3486333 |
chr11:106785042-106790740 |
Weak transcription ZNF genes & repeats Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv556232 |
chr11:106785139-106787540 |
ZNF genes & repeats Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv556233 |
chr11:106785139-106787809 |
Weak transcription Enhancers ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv556234 |
chr11:106785139-106788876 |
Weak transcription ZNF genes & repeats Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv556235 |
chr11:106785139-106789414 |
Weak transcription ZNF genes & repeats Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv556236 |
chr11:106785139-106789492 |
Weak transcription ZNF genes & repeats Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv556237 |
chr11:106785139-106795127 |
Weak transcription Enhancers ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3486336 |
chr11:106785492-106790590 |
Enhancers Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3466208 |
chr11:106785822-106789811 |
Weak transcription Enhancers ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page:
1
