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 |
nsv897094 |
chr11:24761831-24793160 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
4 |
nsv1044583 |
chr11:24772936-24831557 |
Enhancers Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
5 |
nsv553822 |
chr11:24774037-24786653 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
6 |
nsv897095 |
chr11:24774864-24793160 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
7 |
nsv553823 |
chr11:24778111-24788677 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
8 |
nsv897096 |
chr11:24778111-24793160 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|