| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv877332 |
chr3:109575764-110186611 |
Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv460816 |
chr3:109878008-110044601 |
Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv591271 |
chr3:109878008-110044601 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv829668 |
chr3:109956403-110095215 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv877334 |
chr3:109983269-110044601 |
Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv877335 |
chr3:109986271-110061676 |
Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3324546 |
chr3:109991733-109992234 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
