| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv582235 |
chr2:76881210-76997763 |
Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1002822 |
chr2:76885103-76940701 |
Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv1010119 |
chr2:76904730-76949552 |
Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
nsv1003119 |
chr2:76914457-76949552 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv1003325 |
chr2:76914457-76957491 |
Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv998226 |
chr2:76919605-76949552 |
Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv1002481 |
chr2:76919605-76957491 |
Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv1012020 |
chr2:76921092-76946538 |
Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv1011976 |
chr2:76921664-76949315 |
Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv1001059 |
chr2:76921664-76949552 |
Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv1009416 |
chr2:76924371-76949315 |
Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv1009850 |
chr2:76924371-76949552 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv1008460 |
chr2:76928121-76949552 |
Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv1013202 |
chr2:76928121-76956494 |
Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv999909 |
chr2:76928121-76957491 |
Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv582237 |
chr2:76929095-76949101 |
Enhancers Weak transcription ZNF genes & repeats Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv582238 |
chr2:76929095-76949315 |
Enhancers Weak transcription ZNF genes & repeats Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv874318 |
chr2:76929095-76956302 |
Enhancers Weak transcription Active TSS ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv582239 |
chr2:76935514-76948043 |
ZNF genes & repeats Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv582240 |
chr2:76935514-76949315 |
Weak transcription Enhancers ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv582241 |
chr2:76935514-76956302 |
Weak transcription Active TSS Enhancers ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv33650 |
chr2:76935740-76949563 |
Enhancers ZNF genes & repeats Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
nsv1012147 |
chr2:76936019-76957491 |
Enhancers Weak transcription Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv2762679 |
chr2:76936031-76957088 |
Weak transcription Active TSS Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
nsv961672 |
chr2:76938081-76949105 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page:
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