| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv482877 |
chr9:93979351-94157734 |
Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
8 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv893571 |
chr9:94072113-94202927 |
Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
17 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv824980 |
chr9:94131502-94215911 |
Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
14 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv3482520 |
chr9:94148039-94148593 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3500946 |
chr9:94148068-94148569 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3341835 |
chr9:94148081-94148528 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv818712 |
chr9:94148084-94154282 |
Weak transcription Enhancers Flanking Active TSS
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
esv3500947 |
chr9:94148086-94148585 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3500944 |
chr9:94148090-94148587 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3482518 |
chr9:94148110-94148522 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3482521 |
chr9:94148145-94148490 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3500945 |
chr9:94148157-94148501 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3482522 |
chr9:94148161-94148499 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3500948 |
chr9:94148161-94148499 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page:
1
