| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv532233 |
chr12:29009388-29496179 |
Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
18 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv995123 |
chr12:29095272-29571558 |
Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
35 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv2758301 |
chr12:29110782-29289849 |
Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv2759888 |
chr12:29110782-29289849 |
Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv557888 |
chr12:29158183-29163291 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv557889 |
chr12:29158183-29164515 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv557890 |
chr12:29158183-29167983 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3509368 |
chr12:29160485-29165983 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv999221 |
chr12:29160579-29164985 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3484785 |
chr12:29161330-29165138 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
