Variant report
Variant | rs6495306 |
---|---|
Chromosome Location | chr15:78865893-78865894 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000169684 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11632604 | 0.84[CEU][hapmap] |
rs11636131 | 0.84[CEU][hapmap] |
rs11637635 | 0.88[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap];0.95[YRI][hapmap];0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs11858230 | 0.81[CEU][hapmap] |
rs12901300 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs12902493 | 0.84[CEU][hapmap] |
rs12906951 | 0.84[CEU][hapmap] |
rs12907966 | 0.84[CEU][hapmap];0.81[TSI][hapmap] |
rs12910289 | 0.88[CEU][hapmap] |
rs12911602 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs12914694 | 0.84[CEU][hapmap] |
rs12916483 | 0.84[CEU][hapmap];0.81[TSI][hapmap] |
rs12916999 | 0.84[CEU][hapmap] |
rs1504545 | 0.84[CEU][hapmap] |
rs1504546 | 0.84[CEU][hapmap] |
rs17408276 | 0.84[CEU][hapmap] |
rs1878399 | 0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1979905 | 0.84[CEU][hapmap] |
rs1979906 | 0.84[CEU][hapmap];0.81[TSI][hapmap] |
rs1979907 | 0.86[CEU][hapmap] |
rs2292117 | 0.84[CEU][hapmap] |
rs2456019 | 0.81[AMR][1000 genomes] |
rs2869546 | 0.88[CEU][hapmap] |
rs3743073 | 0.83[CEU][hapmap] |
rs3743074 | 0.84[CEU][hapmap];0.87[GIH][hapmap] |
rs3743075 | 0.84[CEU][hapmap];0.87[GIH][hapmap] |
rs3743077 | 0.96[CEU][hapmap];0.84[CHD][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs3813571 | 0.84[CEU][hapmap];0.81[TSI][hapmap] |
rs3813572 | 0.84[CEU][hapmap];0.81[TSI][hapmap] |
rs3829787 | 0.84[ASN][1000 genomes] |
rs4243083 | 0.83[CEU][hapmap] |
rs4275821 | 0.83[CHB][hapmap];0.84[ASN][1000 genomes] |
rs472054 | 0.84[CEU][hapmap];0.82[CHD][hapmap];0.85[GIH][hapmap];0.88[MEX][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs481134 | 0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4886571 | 0.84[CEU][hapmap];0.81[TSI][hapmap] |
rs4887063 | 0.83[CEU][hapmap] |
rs4887064 | 0.84[CEU][hapmap] |
rs495956 | 0.88[CEU][hapmap] |
rs514743 | 0.84[CEU][hapmap];0.82[CHD][hapmap];0.84[GIH][hapmap];0.88[MEX][hapmap];0.81[AMR][1000 genomes] |
rs555018 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs57945453 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs588765 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs601079 | 1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs61012457 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs615470 | 0.84[CEU][hapmap];0.85[GIH][hapmap];0.83[MEX][hapmap] |
rs621849 | 1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs647041 | 0.96[CEU][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6495307 | 0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs660652 | 0.84[CEU][hapmap];0.82[CHD][hapmap];0.85[GIH][hapmap];0.88[MEX][hapmap];0.90[YRI][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs680244 | 1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs692780 | 0.88[CEU][hapmap];0.82[CHB][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs7164030 | 0.84[CEU][hapmap] |
rs7173512 | 0.83[CHB][hapmap];0.84[ASN][1000 genomes] |
rs8025188 | 0.87[EUR][1000 genomes] |
rs8025429 | 0.86[CEU][hapmap] |
rs8053 | 0.84[CEU][hapmap];0.84[GIH][hapmap];0.81[TSI][hapmap] |
rs880395 | 0.84[CEU][hapmap] |
rs905740 | 0.84[CEU][hapmap] |
rs952215 | 0.84[CEU][hapmap] |
rs952216 | 0.83[CEU][hapmap] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv917303 | chr15:78491050-79205255 | Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 122 gene(s) | inside rSNPs | diseases |
2 | nsv1038816 | chr15:78796434-78881087 | Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 48 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs6495306 | PSMA4 | cis | cerebellum | SCAN |
rs6495306 | CHRNA5 | cis | lung | GTEx |
rs6495306 | RP11-650L12.2 | cis | Nerve Tibial | GTEx |
rs6495306 | CHRNA3 | cis | Muscle Skeletal | GTEx |
rs6495306 | RP11-650L12.2 | cis | lung | GTEx |
rs6495306 | IREB2 | cis | cerebellum | SCAN |
rs6495306 | RP11-650L12.2 | cis | Esophagus Mucosa | GTEx |
rs6495306 | CHRNA5 | cis | Esophagus Mucosa | GTEx |
rs6495306 | CHRNA5 | cis | Muscle Skeletal | GTEx |
rs6495306 | CHRNA5 | cis | Adipose Subcutaneous | GTEx |
rs6495306 | RP11-650L12.2 | cis | Adipose Subcutaneous | GTEx |
rs6495306 | CHRNA5 | cis | cerebellum | SCAN |
rs6495306 | RP11-650L12.2 | cis | Muscle Skeletal | GTEx |
rs6495306 | CHRNA5 | cis | Nerve Tibial | GTEx |
rs6495306 | IREB2 | cis | parietal | SCAN |
rs6495306 | CHRNA5 | cis | multi-tissue | Pritchard |
rs6495306 | CHRNA5 | cis | Heart Left Ventricle | GTEx |
rs6495306 | RP11-650L12.2 | cis | Heart Left Ventricle | GTEx |
rs6495306 | CHRNA5 | cis | parietal | SCAN |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:78859000-78868400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr15:78859200-78882400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
3 | chr15:78860200-78881400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
4 | chr15:78860200-78881600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
5 | chr15:78860200-78882200 | Weak transcription | Hela-S3 | cervix |
6 | chr15:78863600-78867200 | Weak transcription | GM12878-XiMat | blood |
7 | chr15:78864600-78869200 | Weak transcription | A549 | lung |
8 | chr15:78865800-78866200 | Enhancers | Fetal Brain Female | brain |
9 | chr15:78865800-78873200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |