| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv874317 |
chr2:76554077-76890567 |
Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv1800238 |
chr2:76746272-76786845 |
Weak transcription Enhancers Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv1803934 |
chr2:76746272-76786845 |
Enhancers Flanking Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv1804555 |
chr2:76746272-76786845 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv1805818 |
chr2:76746272-76786845 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv1820531 |
chr2:76746272-76786845 |
Enhancers Flanking Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv1822967 |
chr2:76746272-76786845 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv1834518 |
chr2:76746272-76786845 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv1840522 |
chr2:76746272-76786845 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv1801302 |
chr2:76764537-76789625 |
Flanking Active TSS Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv1814841 |
chr2:76764537-76789625 |
Enhancers Flanking Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv1005528 |
chr2:76769672-76776464 |
Enhancers Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3456957 |
chr2:76771644-76777342 |
Enhancers Flanking Active TSS Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3333969 |
chr2:76772394-76776892 |
Weak transcription Enhancers Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3456958 |
chr2:76772469-76776817 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3426062 |
chr2:76772744-76776492 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv2479042 |
chr2:76772898-76776225 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv511791 |
chr2:76773094-76776050 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3456960 |
chr2:76773094-76776092 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv1822709 |
chr2:76773793-76777279 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv582231 |
chr2:76773957-76780130 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page:
1
