| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1047488 |
chr13:84629304-84696148 |
Weak transcription Active TSS Enhancers ZNF genes & repeats
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
nsv1046982 |
chr13:84631965-84800765 |
Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv1038880 |
chr13:84632431-84861839 |
Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv949402 |
chr13:84675752-85606846 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv1035493 |
chr13:84683545-84779862 |
Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv900687 |
chr13:84691001-84714655 |
Enhancers Weak transcription Flanking Active TSS Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
