| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv3328565 |
chr3:27991169-28915035 |
Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
28 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv876648 |
chr3:28060456-28280965 |
Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
8 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv876649 |
chr3:28126595-28718454 |
Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
27 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv508214 |
chr3:28157554-28198530 |
Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer
|
Chromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv2502603 |
chr3:28167062-28168554 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv1976373 |
chr3:28167268-28167956 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3498638 |
chr3:28167314-28167891 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3463299 |
chr3:28167343-28167839 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3498637 |
chr3:28167358-28167876 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3498635 |
chr3:28167367-28167834 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3463296 |
chr3:28167388-28167849 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3463295 |
chr3:28167399-28167852 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3463297 |
chr3:28167441-28167790 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3498636 |
chr3:28167452-28167805 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3463300 |
chr3:28167457-28167800 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3498639 |
chr3:28167457-28167800 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv1570870 |
chr3:28167473-28167799 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page:
1
