No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1065969 |
chr20:10850562-11464172 |
Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers
|
TF binding regionChromatin interactive regionlncRNA
|
11 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv544181 |
chr20:10850562-11464172 |
Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers
|
TF binding regionChromatin interactive regionlncRNA
|
11 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv432099 |
chr20:11371093-11476900 |
Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
4 |
nsv1061567 |
chr20:11379484-11405302 |
Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
5 |
nsv1058734 |
chr20:11389232-11479953 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv1067948 |
chr20:11390582-11390583 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
7 |
nsv172171 |
chr20:11390583-11390583 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|