| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1031071 |
chr7:144318082-145125392 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
20 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv539169 |
chr7:144318082-145125392 |
Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
20 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv831179 |
chr7:144830077-144998851 |
Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
5 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv1026420 |
chr7:144902627-145020612 |
Enhancers Weak transcription ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv3506044 |
chr7:144915719-144922517 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3506043 |
chr7:144916169-144922467 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv1007031 |
chr7:144916246-144921563 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3476905 |
chr7:144916750-144921511 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3420768 |
chr7:144916798-144921494 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3476903 |
chr7:144916801-144921483 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3506041 |
chr7:144916802-144921455 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3476904 |
chr7:144916812-144921500 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3476906 |
chr7:144916820-144921443 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3506045 |
chr7:144916827-144921455 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3506042 |
chr7:144916827-144921458 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3353115 |
chr7:144916845-144921420 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv365422 |
chr7:144916882-144921398 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3476907 |
chr7:144916882-144921402 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page:
1
