| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv932 |
chr1:56816732-56842261 |
Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
esv3509488 |
chr1:56829121-56835877 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv3344758 |
chr1:56830514-56836162 |
Enhancers Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3320001 |
chr1:56830662-56835297 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv8427 |
chr1:56830839-56835252 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv508204 |
chr1:56830844-56840857 |
Flanking Active TSS Enhancers Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3509491 |
chr1:56830995-56835053 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3509487 |
chr1:56831008-56835715 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3509492 |
chr1:56831014-56835077 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3320003 |
chr1:56831029-56835067 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3509486 |
chr1:56831038-56834998 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv1005520 |
chr1:56831042-56839645 |
Enhancers Weak transcription Flanking Active TSS Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3320005 |
chr1:56831045-56835032 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3320006 |
chr1:56831047-56835033 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page:
1
