| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv460919 |
chr3:161799090-162094430 |
Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv592144 |
chr3:161799090-162094430 |
Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv877713 |
chr3:161807012-161847016 |
Enhancers Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv877714 |
chr3:161807012-161854219 |
Enhancers Flanking Active TSS Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv877715 |
chr3:161807012-161862628 |
Enhancers Weak transcription Flanking Active TSS Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv12869 |
chr3:161808602-161816680 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
