| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1014232 |
chr2:78413760-79034119 |
Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv535788 |
chr2:78413760-79034119 |
Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv916498 |
chr2:78429997-79340383 |
Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
8 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv582273 |
chr2:78432494-78978011 |
Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv3584761 |
chr2:78545020-79430628 |
Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
13 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv998961 |
chr2:78574081-79150087 |
Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv428052 |
chr2:78615333-79075603 |
Enhancers ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
nsv874370 |
chr2:78668935-79013457 |
Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 9 |
esv2755345 |
chr2:78857845-79045945 |
Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv874373 |
chr2:78914837-79010908 |
Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3518771 |
chr2:78970346-78994041 |
Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3518772 |
chr2:78970346-78994041 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3514025 |
chr2:78975194-78979992 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3489566 |
chr2:78975844-78979942 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3459636 |
chr2:78976489-78979047 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3459637 |
chr2:78976489-78979047 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3459635 |
chr2:78976492-78979070 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3489568 |
chr2:78976544-78979015 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3514023 |
chr2:78976548-78979004 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3514024 |
chr2:78976564-78978955 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3489567 |
chr2:78976598-78978954 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3514026 |
chr2:78976598-78978955 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3489565 |
chr2:78976641-78978787 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv3489569 |
chr2:78976641-78978787 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv14858 |
chr2:78976660-78978915 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page:
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