| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1043206 |
chr13:89296779-89417347 |
Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
nsv900819 |
chr13:89302824-89405660 |
Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv900820 |
chr13:89302824-89686507 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv900821 |
chr13:89302824-89941209 |
Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
9 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv1037296 |
chr13:89355045-89461651 |
Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv1112 |
chr13:89364975-89417543 |
Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv900822 |
chr13:89397027-89488821 |
Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
