| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1022578 |
chr7:48244414-48584664 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1023575 |
chr7:48244414-48586685 |
Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv1015183 |
chr7:48244414-48588598 |
Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv830992 |
chr7:48497408-48686442 |
Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv888008 |
chr7:48568425-48652224 |
Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv2764056 |
chr7:48580914-48592025 |
Enhancers Strong transcription Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv11768 |
chr7:48581423-48592171 |
Weak transcription Enhancers Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv514416 |
chr7:48581830-48592050 |
Enhancers Weak transcription Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv1818564 |
chr7:48581852-48592025 |
Strong transcription Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv2421774 |
chr7:48581852-48592025 |
Enhancers Weak transcription Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv442042 |
chr7:48581852-48592025 |
Weak transcription Strong transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page:
1
