No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv889083 |
chr7:117203417-117256374 |
Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv889086 |
chr7:117214089-117252873 |
Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
3 |
esv3437516 |
chr7:117252049-117252113 |
Weak transcription Genic enhancers Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
4 |
esv1650978 |
chr7:117252094-117252108 |
Strong transcription Weak transcription Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|