Variant report
Variant | rs12354802 |
---|---|
Chromosome Location | chr10:45728360-45728361 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:45495502..45498143-chr10:45727640..45729872,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000165512 | Chromatin interaction |
ENSG00000165511 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10159580 | 1.00[CHB][hapmap] |
rs10900197 | 1.00[CHB][hapmap] |
rs11239396 | 0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11239398 | 0.83[EUR][1000 genomes] |
rs11239436 | 1.00[CHB][hapmap] |
rs11239437 | 1.00[CHB][hapmap] |
rs11239501 | 1.00[CHB][hapmap] |
rs11239515 | 1.00[CHB][hapmap] |
rs11239516 | 1.00[CHB][hapmap] |
rs1339746 | 1.00[CHB][hapmap] |
rs17157583 | 0.83[EUR][1000 genomes] |
rs17157619 | 0.83[EUR][1000 genomes] |
rs17157697 | 1.00[CHB][hapmap] |
rs17444064 | 1.00[CHB][hapmap] |
rs17520779 | 0.80[EUR][1000 genomes] |
rs1815626 | 0.83[EUR][1000 genomes] |
rs2211163 | 1.00[CHB][hapmap] |
rs7085353 | 1.00[CHB][hapmap] |
rs72784518 | 0.83[EUR][1000 genomes] |
rs7895871 | 0.82[EUR][1000 genomes] |
rs7898796 | 0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2750897 | chr10:45550145-45820136 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv895105 | chr10:45636867-45928822 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv430166 | chr10:45668894-46148794 | Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
4 | esv2595492 | chr10:45728107-45732276 | Weak transcription Flanking Active TSS Enhancers Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |