| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv885900 |
chr6:54517968-54852462 |
Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
13 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv1813954 |
chr6:54518364-54557296 |
Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv1813136 |
chr6:54550530-54557193 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv1807602 |
chr6:54553140-54557193 |
Bivalent Enhancer Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3473995 |
chr6:54553738-54557493 |
Enhancers Weak transcription Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3473997 |
chr6:54553854-54557380 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv21159 |
chr6:54553918-54557383 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv1804920 |
chr6:54553922-54557399 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv1811098 |
chr6:54553922-54557399 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv1805121 |
chr6:54553942-54557193 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv1805171 |
chr6:54553942-54557193 |
Weak transcription Bivalent Enhancer Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv1809635 |
chr6:54553942-54557193 |
Bivalent Enhancer Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv1812631 |
chr6:54553942-54557193 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv1804438 |
chr6:54554122-54557296 |
Enhancers Bivalent Enhancer Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv1805482 |
chr6:54554122-54557296 |
Bivalent Enhancer Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv1812353 |
chr6:54554502-54557193 |
Bivalent Enhancer Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv2510453 |
chr6:54555535-54557066 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3414743 |
chr6:54555743-54557741 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv9697 |
chr6:54556187-54556998 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv1963826 |
chr6:54556249-54556975 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3472592 |
chr6:54556329-54556856 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3522115 |
chr6:54556342-54556858 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3522116 |
chr6:54556344-54556875 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv4232 |
chr6:54556381-54556954 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv3522113 |
chr6:54556394-54556848 |
Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page:
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