| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv428069 |
chr2:187575692-187766209 |
ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3495864 |
chr2:187633495-187686087 |
Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv3495865 |
chr2:187633495-187686087 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv3446718 |
chr2:187663495-187686087 |
Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3345821 |
chr2:187663495-187692736 |
Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3509137 |
chr2:187673557-187677655 |
Enhancers Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3509138 |
chr2:187673957-187677555 |
Enhancers Active TSS Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 8 |
esv3459914 |
chr2:187674495-187676681 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 9 |
esv3509135 |
chr2:187674529-187676734 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 10 |
esv3509134 |
chr2:187674542-187676605 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 11 |
esv3459912 |
chr2:187674555-187676611 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 12 |
esv3509136 |
chr2:187674588-187676672 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 13 |
esv3459913 |
chr2:187674633-187676520 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 14 |
esv3509139 |
chr2:187674643-187676524 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 15 |
esv3459915 |
chr2:187674647-187676522 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 16 |
esv3509140 |
chr2:187674647-187676522 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page:
1
