No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
esv1796184 |
chr3:100507827-100522384 |
Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
2 |
nsv591170 |
chr3:100514481-100522220 |
Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
3 |
esv1795329 |
chr3:100514481-100522384 |
Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
4 |
esv1803695 |
chr3:100514481-100522384 |
Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
5 |
nsv591171 |
chr3:100516767-100522220 |
Enhancers Weak transcription Genic enhancers Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
6 |
nsv591172 |
chr3:100516767-100522384 |
Weak transcription Enhancers Genic enhancers Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|