| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv878741 |
chr4:20440476-20486230 |
Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
esv3342251 |
chr4:20472879-20475427 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv3420326 |
chr4:20473054-20475202 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3356552 |
chr4:20473554-20474802 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3382575 |
chr4:20473719-20474101 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv878742 |
chr4:20473799-20527864 |
Weak transcription Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv255583 |
chr4:20473939-20473940 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
