| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv497859 |
chr10:96058024-97027747 |
Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
41 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv529726 |
chr10:96632494-97106315 |
Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
15 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv21432 |
chr10:96856006-96996043 |
Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv517863 |
chr10:96904057-96928702 |
Weak transcription Enhancers ZNF genes & repeats
|
TF binding regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv3396941 |
chr10:96921262-96925460 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
