| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv998949 |
chr3:158774806-159394550 |
Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv877696 |
chr3:159184569-159257961 |
Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv877697 |
chr3:159198139-159259124 |
Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv519199 |
chr3:159248823-159259124 |
Enhancers Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv511197 |
chr3:159252752-159257961 |
Enhancers Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv513091 |
chr3:159254887-159257753 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3462777 |
chr3:159255058-159259656 |
Enhancers
|
lncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3489704 |
chr3:159256308-159258706 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3462778 |
chr3:159256694-159258374 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3462775 |
chr3:159256888-159257798 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv820265 |
chr3:159256894-159257869 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3489706 |
chr3:159256908-159257812 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3489709 |
chr3:159256916-159257800 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3489705 |
chr3:159256932-159257727 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3462779 |
chr3:159256944-159257764 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3462773 |
chr3:159256953-159257769 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3462776 |
chr3:159256955-159257718 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3489708 |
chr3:159256959-159257746 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv822303 |
chr3:159256978-159257652 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv821438 |
chr3:159256978-159257696 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv822304 |
chr3:159256978-159257696 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv4370 |
chr3:159256979-159257791 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page:
1
