| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv530038 |
chr14:37590543-38336191 |
Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
58 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv916985 |
chr14:38052347-38838551 |
Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
59 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv564383 |
chr14:38223275-38262762 |
Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers
|
TF binding regionCpG island
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv564384 |
chr14:38233493-38262762 |
Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers
|
TF binding regionCpG island
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv2161720 |
chr14:38245038-38245646 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv6595 |
chr14:38245131-38245533 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3519608 |
chr14:38245144-38245553 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3519606 |
chr14:38245148-38245571 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3519609 |
chr14:38245163-38245508 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3519605 |
chr14:38245168-38245490 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3528507 |
chr14:38245178-38245524 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3528529 |
chr14:38245179-38245522 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3327814 |
chr14:38245180-38245504 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3528495 |
chr14:38245189-38245479 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv4501 |
chr14:38245194-38245509 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3367590 |
chr14:38245200-38245474 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3519610 |
chr14:38245231-38245473 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3421996 |
chr14:38245401-38249799 |
Active TSS Genic enhancers ZNF genes & repeats Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page:
1
