| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv900790 |
chr13:88585928-88891870 |
Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv900791 |
chr13:88623302-88771495 |
Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv900792 |
chr13:88623302-88871759 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv900793 |
chr13:88711960-88871759 |
Enhancers Weak transcription Active TSS Flanking Active TSS
|
TF binding regionCpG islandlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv983762 |
chr13:88726553-88757094 |
Weak transcription Enhancers Flanking Active TSS
|
lncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv1037729 |
chr13:88728499-89127873 |
Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv541864 |
chr13:88728499-89127873 |
Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page:
1
