No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv895565 |
chr10:61347537-61379398 |
Weak transcription Enhancers Flanking Active TSS Active TSS
|
TF binding regionChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv895566 |
chr10:61350192-61379398 |
Weak transcription Enhancers Active TSS Flanking Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
3 |
nsv437684 |
chr10:61354446-61367720 |
Enhancers Weak transcription
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
4 |
nsv437683 |
chr10:61354446-61369980 |
Weak transcription Enhancers Flanking Active TSS Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
5 |
esv1385689 |
chr10:61355743-61355744 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|