| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv869971 |
chr7:117420583-118274149 |
Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
40 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv889088 |
chr7:117744660-117913648 |
Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
25 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv889089 |
chr7:117865940-117921267 |
Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats
|
TF binding regionChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv889090 |
chr7:117865940-118067460 |
Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv2432841 |
chr7:117893381-117895064 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 6 |
esv3362740 |
chr7:117893541-117895689 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 7 |
esv1993322 |
chr7:117893760-117894466 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 8 |
esv3476668 |
chr7:117893859-117894339 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 9 |
esv3496070 |
chr7:117893868-117894365 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 10 |
esv3496073 |
chr7:117893875-117894354 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 11 |
esv3496071 |
chr7:117893889-117894289 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 12 |
esv4194 |
chr7:117893891-117894297 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 13 |
esv3476669 |
chr7:117893894-117894305 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 14 |
esv3496069 |
chr7:117893900-117894310 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 15 |
esv3476666 |
chr7:117893900-117894320 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 16 |
esv3476667 |
chr7:117893910-117894257 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 17 |
esv3496068 |
chr7:117893913-117894299 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 18 |
esv3383648 |
chr7:117893916-117894276 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 19 |
esv3476665 |
chr7:117893937-117894257 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 20 |
esv3496072 |
chr7:117893947-117894272 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 21 |
esv1542537 |
chr7:117893950-117894252 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 22 |
esv3476670 |
chr7:117893951-117894270 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 23 |
esv3496075 |
chr7:117893951-117894270 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 24 |
esv1005404 |
chr7:117893954-117894255 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 25 |
esv2557418 |
chr7:117893958-117894259 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page:
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