| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv899369 |
chr12:84536107-85067814 |
Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
10 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1035863 |
chr12:84710250-85331290 |
Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
17 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv1035236 |
chr12:84790507-85350433 |
Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
18 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv899373 |
chr12:84891803-84999922 |
Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS
|
Chromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv1039601 |
chr12:84926324-84984595 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3388412 |
chr12:84947780-84948201 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
