| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv497867 |
chr12:41286305-41728650 |
Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv899034 |
chr12:41515090-41698342 |
Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv899035 |
chr12:41548545-41710912 |
Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv469364 |
chr12:41631105-41710912 |
Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 5 |
nsv558699 |
chr12:41631105-41710912 |
Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 6 |
nsv517338 |
chr12:41653979-41662453 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
