| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1013712 |
chr2:234558457-235495825 |
Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
41 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv532476 |
chr2:234595695-235134381 |
Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
37 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv1811811 |
chr2:234633964-234709430 |
Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
16 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv527330 |
chr2:234688036-234702905 |
Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv584706 |
chr2:234698097-234699242 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
esv10212 |
chr2:234698279-234701274 |
Enhancers
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
esv11552 |
chr2:234698752-234699856 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
nsv584707 |
chr2:234698776-234699346 |
Inactive region
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 9 |
esv3488412 |
chr2:234698909-234699450 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 10 |
esv3488413 |
chr2:234698909-234699450 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 11 |
esv3460957 |
chr2:234698963-234699429 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 12 |
esv3331186 |
chr2:234698991-234699462 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 13 |
esv2332178 |
chr2:234698995-234699471 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 14 |
esv3427806 |
chr2:234699010-234699428 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 15 |
esv3372604 |
chr2:234699016-234699402 |
Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page:
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