No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv893589 |
chr9:96624645-96884544 |
Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
18 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv1046904 |
chr9:96647940-96689327 |
Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
5 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv1035418 |
chr9:96647940-96711409 |
Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription
|
Chromatin interactive region
|
5 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv1042043 |
chr9:96657324-96689327 |
Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|