| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1014941 |
chr4:20611726-21345226 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
7 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv537053 |
chr4:20611726-21345226 |
ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
7 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv1013365 |
chr4:20834054-21609078 |
Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv878746 |
chr4:21054348-21169062 |
Enhancers Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv878747 |
chr4:21057794-21169062 |
Enhancers Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv878748 |
chr4:21113871-21169062 |
Enhancers Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv4264 |
chr4:21138131-21199262 |
Weak transcription Enhancers Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3430970 |
chr4:21159504-21168002 |
Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv1005654 |
chr4:21159672-21167100 |
Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv1010273 |
chr4:21160249-21177683 |
Enhancers Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv513123 |
chr4:21160314-21167128 |
Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv2637742 |
chr4:21160408-21167871 |
Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3499301 |
chr4:21160522-21167796 |
Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3464880 |
chr4:21160657-21167336 |
Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv436408 |
chr4:21160662-21167279 |
Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv435801 |
chr4:21160692-21167021 |
Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv2318387 |
chr4:21160802-21167317 |
Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3499303 |
chr4:21160871-21167216 |
Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3499302 |
chr4:21160879-21167216 |
Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page:
1
