| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv869450 |
chrX:29433295-29940875 |
Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription
|
TF binding regionChromatin interactive regionlncRNAmiRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv869408 |
chrX:29619835-30341063 |
Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
10 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv3334028 |
chrX:29928156-30104332 |
Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS
|
TF binding regionCpG islandlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv3401634 |
chrX:29933931-29989429 |
Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
