| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv530933 |
chr9:16251206-16830845 |
Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
13 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv530934 |
chr9:16281246-16779432 |
Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
13 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv466264 |
chr9:16359608-16390629 |
Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats
|
lncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv613669 |
chr9:16359608-16390629 |
Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS
|
lncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv2462705 |
chr9:16389073-16390515 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv9441 |
chr9:16389154-16389970 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv2413865 |
chr9:16389207-16389924 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3339110 |
chr9:16389295-16389808 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3495011 |
chr9:16389299-16389833 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3495014 |
chr9:16389306-16389820 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3495016 |
chr9:16389319-16389784 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3495013 |
chr9:16389321-16389766 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3482014 |
chr9:16389337-16389797 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3495015 |
chr9:16389338-16389782 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3482011 |
chr9:16389338-16389792 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3190 |
chr9:16389339-16389867 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3482013 |
chr9:16389344-16389756 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3495012 |
chr9:16389353-16389765 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3349443 |
chr9:16389358-16389752 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3482012 |
chr9:16389379-16389738 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3495010 |
chr9:16389394-16389731 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
nsv416795 |
chr9:16389395-16389730 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3482015 |
chr9:16389395-16389744 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv3495017 |
chr9:16389395-16389744 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv1006629 |
chr9:16389398-16389731 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
esv2571946 |
chr9:16389404-16389739 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
esv1622328 |
chr9:16389407-16389743 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
nsv416318 |
chr9:16389408-16389743 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page:
1
