| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv3388948 |
chr2:50092667-50602681 |
Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3399511 |
chr2:50092687-50602651 |
Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv934303 |
chr2:50145598-50412189 |
Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv581837 |
chr2:50230334-50268616 |
Weak transcription Flanking Active TSS Enhancers
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv1011144 |
chr2:50231111-50270096 |
Enhancers Flanking Active TSS Weak transcription
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv915588 |
chr2:50235306-50268306 |
Enhancers Weak transcription
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv431002 |
chr2:50243349-50259749 |
Enhancers Weak transcription
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
esv3354044 |
chr2:50245898-50248196 |
Enhancers
|
TF binding region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page:
1
