No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1052730 |
chr11:24695821-25272497 |
Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv1053055 |
chr11:24700012-25293551 |
Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv1044583 |
chr11:24772936-24831557 |
Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv897098 |
chr11:24778459-24814076 |
Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
5 |
nsv469946 |
chr11:24778961-24795275 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
6 |
nsv467757 |
chr11:24778961-24803061 |
Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
7 |
nsv553826 |
chr11:24778961-24803061 |
Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
8 |
nsv897099 |
chr11:24783183-24814076 |
Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
9 |
esv3345962 |
chr11:24795126-24797474 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|