| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv833641 |
chr18:44815063-45020202 |
Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionChromatin interactive regionlncRNAmiRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv1801141 |
chr18:44908270-44955409 |
Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv21357 |
chr18:44925360-44928518 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3505306 |
chr18:44925654-44930052 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3505309 |
chr18:44926229-44930077 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3375590 |
chr18:44926479-44929327 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv16703 |
chr18:44926638-44929859 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv820911 |
chr18:44926638-44929859 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3505308 |
chr18:44926760-44929006 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3505310 |
chr18:44926760-44929006 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv1810690 |
chr18:44926844-44929301 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv1815121 |
chr18:44926844-44929301 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3424433 |
chr18:44926929-44928753 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv1303557 |
chr18:44927273-44927899 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page:
1
