No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
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
|
2 |
esv3466297 |
chr11:106878461-106879112 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
3 |
esv3466286 |
chr11:106878514-106879082 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
4 |
esv3466274 |
chr11:106878531-106879035 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
5 |
esv3466308 |
chr11:106878582-106878982 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
6 |
esv3466319 |
chr11:106878596-106878980 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|