| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv932168 |
chr7:15573437-15895294 |
Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
10 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv523199 |
chr7:15582208-16042596 |
Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
11 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv606299 |
chr7:15603853-15637887 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv887735 |
chr7:15625992-15698178 |
Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh
|
Chromatin interactive regionlncRNAmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv606300 |
chr7:15630754-15637713 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv606301 |
chr7:15630871-15636977 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv606302 |
chr7:15630871-15637005 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv606303 |
chr7:15630871-15637403 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv606304 |
chr7:15630871-15637565 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv15969 |
chr7:15635015-15638178 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv606305 |
chr7:15635995-15637005 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv606306 |
chr7:15635995-15637565 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv606307 |
chr7:15635995-15637713 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv606308 |
chr7:15636259-15637880 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv606309 |
chr7:15636352-15637565 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page:
1
