| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1013820 |
chr3:82175705-82968181 |
Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
11 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv2830308 |
chr3:82741198-83269730 |
Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv1805592 |
chr3:82853590-82913445 |
ZNF genes & repeats Enhancers Weak transcription
|
TF binding regionCpG island
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv1814571 |
chr3:82857229-82910711 |
ZNF genes & repeats Enhancers Weak transcription
|
TF binding regionCpG island
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv1805787 |
chr3:82863216-82910711 |
Enhancers ZNF genes & repeats Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv1811868 |
chr3:82863216-82913445 |
ZNF genes & repeats Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv1807406 |
chr3:82867767-82888913 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 8 |
esv1811614 |
chr3:82867767-82888913 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 9 |
esv1814226 |
chr3:82867892-82888913 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 10 |
esv1812004 |
chr3:82867892-82913445 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv590796 |
chr3:82869029-82903161 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv1805273 |
chr3:82869089-82910711 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv877046 |
chr3:82869089-82982088 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv877047 |
chr3:82869089-83027612 |
Enhancers Weak transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv877048 |
chr3:82869089-83324183 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv1809393 |
chr3:82869272-82888913 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 17 |
nsv590802 |
chr3:82871009-82896772 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 18 |
nsv590803 |
chr3:82871009-82903161 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv877049 |
chr3:82873604-82927941 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv877050 |
chr3:82873604-83012312 |
ZNF genes & repeats Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv590804 |
chr3:82882974-82927941 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page:
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