| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv2752691 |
chr10:57738694-58541894 |
Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
9 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1039709 |
chr10:58343941-58522183 |
Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv540649 |
chr10:58343941-58522183 |
Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv2753387 |
chr10:58434394-58510694 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv427866 |
chr10:58448655-58548655 |
Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv551064 |
chr10:58457011-58702440 |
Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv2754330 |
chr10:58477451-58511952 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv2756467 |
chr10:58489294-58511952 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv2758223 |
chr10:58490630-58689953 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv2759758 |
chr10:58490630-58689953 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv437117 |
chr10:58497570-58531235 |
Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv470948 |
chr10:58498060-58519258 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv947639 |
chr10:58500054-58513799 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv895505 |
chr10:58500057-58517273 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv551065 |
chr10:58501922-58517273 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv8672 |
chr10:58503626-58507400 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 17 |
nsv551066 |
chr10:58503786-58509354 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page:
1
