| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv882729 |
chr5:113743628-114497708 |
Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
9 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv830452 |
chr5:113798617-113975228 |
Enhancers Strong transcription Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv1020798 |
chr5:113821828-114392727 |
Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv537867 |
chr5:113821828-114392727 |
Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv1023944 |
chr5:113925779-113976017 |
Bivalent/Poised TSS Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv1034890 |
chr5:113925779-113977959 |
Bivalent/Poised TSS Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv1015654 |
chr5:113928284-113976017 |
Enhancers Bivalent/Poised TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv1020870 |
chr5:113928284-113980156 |
Enhancers Bivalent/Poised TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv1019344 |
chr5:113935819-114021552 |
Enhancers Weak transcription Bivalent/Poised TSS
|
TF binding regionChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
