| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv497867 |
chr12:41286305-41728650 |
Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv832382 |
chr12:41359550-41489681 |
Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv427910 |
chr12:41374913-41650593 |
Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv428587 |
chr12:41375635-41546845 |
Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv1051524 |
chr12:41409977-41643387 |
Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
esv3333180 |
chr12:41471734-41494699 |
Enhancers Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 7 |
esv3487733 |
chr12:41482858-41483191 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 8 |
esv3487734 |
chr12:41482878-41483148 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 9 |
esv3501963 |
chr12:41482978-41483082 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 10 |
esv3487732 |
chr12:41482988-41483082 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 11 |
esv3487735 |
chr12:41482992-41483080 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 12 |
esv3501974 |
chr12:41482992-41483080 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page:
1
