| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv3343291 |
chr12:30455597-30992837 |
Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
48 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv832361 |
chr12:30794030-30997241 |
Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
41 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv949148 |
chr12:30800040-31131712 |
Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
45 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv3371244 |
chr12:30916285-30920583 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv8803 |
chr12:30918071-30919002 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv820923 |
chr12:30918135-30918781 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
esv3485351 |
chr12:30918153-30918899 |
Weak transcription Enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
esv3485373 |
chr12:30918210-30918865 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3485362 |
chr12:30918218-30918860 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3485340 |
chr12:30918226-30918818 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3140 |
chr12:30918239-30918844 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3485384 |
chr12:30918286-30918793 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv1001294 |
chr12:30918340-30918781 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv826300 |
chr12:30918340-30918781 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page:
1
