| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv998949 |
chr3:158774806-159394550 |
Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv877695 |
chr3:159152259-159254385 |
Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv877696 |
chr3:159184569-159257961 |
Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv877697 |
chr3:159198139-159259124 |
Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv519199 |
chr3:159248823-159259124 |
Enhancers Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv511197 |
chr3:159252752-159257961 |
Enhancers Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
