| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv825385 |
chr10:54878972-54950501 |
Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
nsv825386 |
chr10:54883463-54951261 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv2752952 |
chr10:54900994-55497594 |
Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv831878 |
chr10:54902106-55085586 |
Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv971911 |
chr10:54922353-54950931 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 6 |
nsv1047824 |
chr10:54922737-54948553 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 7 |
nsv1037714 |
chr10:54924559-54948553 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 8 |
esv2764169 |
chr10:54925318-54941401 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 9 |
esv2760126 |
chr10:54927527-54948565 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 10 |
nsv975038 |
chr10:54928027-54938782 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 11 |
esv3315097 |
chr10:54928970-54938274 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 12 |
esv3315108 |
chr10:54928970-54938274 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 13 |
nsv467203 |
chr10:54929003-54955296 |
Weak transcription Active TSS Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 14 |
nsv550927 |
chr10:54929003-54955296 |
Enhancers Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 15 |
esv14013 |
chr10:54929338-54938105 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 16 |
esv34701 |
chr10:54929854-54937494 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 17 |
nsv442575 |
chr10:54929854-54939149 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 18 |
esv2421921 |
chr10:54929854-54939153 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 19 |
nsv1040274 |
chr10:54929854-54964636 |
Weak transcription Enhancers ZNF genes & repeats Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 20 |
esv2755632 |
chr10:54929894-54937494 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 21 |
nsv514558 |
chr10:54930002-54938158 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 22 |
nsv1054455 |
chr10:54932474-55001559 |
Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page:
1
