No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv1054847 |
chr11:4642875-5200656 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
72 gene(s)
|
inside rSNPs
|
diseases
|
2 |
esv2758254 |
chr11:4907893-5135331 |
Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
42 gene(s)
|
inside rSNPs
|
diseases
|
3 |
esv2759799 |
chr11:4907893-5135331 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
42 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv7652 |
chr11:4946245-4997769 |
Enhancers Flanking Active TSS Weak transcription
|
TF binding regionCpG islandChromatin interactive region
|
19 gene(s)
|
inside rSNPs
|
diseases
|
5 |
nsv1052130 |
chr11:4948148-4974017 |
Flanking Active TSS Enhancers
|
TF binding regionChromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|
6 |
nsv1049277 |
chr11:4948160-4974017 |
Enhancers Flanking Active TSS
|
TF binding regionChromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|
7 |
nsv1036758 |
chr11:4948560-4974017 |
Enhancers Flanking Active TSS
|
TF binding regionChromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|