No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1045395 |
chr13:93248456-93323269 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
2 |
nsv456071 |
chr13:93279563-93377562 |
Enhancers Weak transcription Flanking Active TSS Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv562745 |
chr13:93279563-93377562 |
Enhancers Weak transcription Active TSS Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
4 |
esv18734 |
chr13:93279898-93352628 |
Flanking Active TSS Weak transcription Enhancers Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
5 |
nsv983702 |
chr13:93291025-93353518 |
Enhancers Weak transcription Active TSS Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv3348131 |
chr13:93315126-93317224 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
7 |
esv3337875 |
chr13:93315551-93316799 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
8 |
nsv974135 |
chr13:93316448-93318889 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|