No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
esv3508211 |
chr3:159460683-159464431 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
2 |
esv3463577 |
chr3:159461238-159463577 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
3 |
esv3508213 |
chr3:159461273-159463556 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
4 |
esv3508209 |
chr3:159461278-159463532 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
5 |
esv3463578 |
chr3:159461291-159463543 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
6 |
nsv818181 |
chr3:159461456-159466206 |
Enhancers Weak transcription Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
7 |
nsv963569 |
chr3:159462963-159467316 |
Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|