| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv817379 |
chr8:114338391-115011632 |
Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv818650 |
chr8:114574863-115477600 |
Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
7 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv2758168 |
chr8:114575703-115321957 |
Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
7 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv2759636 |
chr8:114575703-115321957 |
Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
7 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv891337 |
chr8:114776941-114882527 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv891340 |
chr8:114828429-115445405 |
Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv891341 |
chr8:114842819-114904731 |
Flanking Bivalent TSS/Enh Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv891342 |
chr8:114846027-114904731 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv818651 |
chr8:114848963-114900567 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv465770 |
chr8:114853127-114897615 |
Flanking Bivalent TSS/Enh Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv611956 |
chr8:114853127-114897615 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv465771 |
chr8:114853127-114900567 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv465773 |
chr8:114853127-114900567 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv611957 |
chr8:114853127-114900567 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv465774 |
chr8:114853127-114907402 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv611958 |
chr8:114853127-114907402 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv891343 |
chr8:114858878-114904731 |
Enhancers Flanking Bivalent TSS/Enh
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv429933 |
chr8:114863824-115049824 |
Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 19 |
nsv470228 |
chr8:114869565-114900567 |
Flanking Bivalent TSS/Enh Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv465775 |
chr8:114869565-114907402 |
Enhancers Flanking Bivalent TSS/Enh
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv611959 |
chr8:114869565-114907402 |
Enhancers Flanking Bivalent TSS/Enh
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
nsv611960 |
chr8:114875165-114908475 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page:
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