No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1004358 |
chr3:133014772-133025177 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
2 |
esv2760760 |
chr3:133014772-133025189 |
Weak transcription Enhancers Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv1006173 |
chr3:133015093-133025177 |
Weak transcription Enhancers Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv4016 |
chr3:133015463-133032477 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
5 |
esv12956 |
chr3:133016100-133025982 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
6 |
nsv514168 |
chr3:133016526-133023166 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|