Variant report
Variant | rs7962411 |
---|---|
Chromosome Location | chr12:85405662-85405663 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10160886 | 0.91[ASN][1000 genomes] |
rs1031190 | 0.96[EUR][1000 genomes] |
rs10862955 | 0.97[ASN][1000 genomes] |
rs11116686 | 0.84[ASN][1000 genomes] |
rs11116701 | 0.97[ASN][1000 genomes] |
rs11116704 | 0.97[ASN][1000 genomes] |
rs11532387 | 0.95[ASN][1000 genomes] |
rs12229124 | 0.98[ASN][1000 genomes] |
rs12229923 | 0.99[ASN][1000 genomes] |
rs12301980 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12304556 | 0.94[EUR][1000 genomes] |
rs12817187 | 0.91[ASN][1000 genomes] |
rs1404867 | 0.99[ASN][1000 genomes] |
rs1404868 | 0.99[ASN][1000 genomes] |
rs1404871 | 0.85[EUR][1000 genomes] |
rs1494500 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1494501 | 0.81[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1525548 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs168615 | 0.88[EUR][1000 genomes] |
rs1690835 | 0.91[EUR][1000 genomes] |
rs17012522 | 0.99[ASN][1000 genomes] |
rs1838671 | 0.99[ASN][1000 genomes] |
rs1852148 | 0.89[EUR][1000 genomes] |
rs1973816 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1976270 | 0.99[ASN][1000 genomes] |
rs2056638 | 0.83[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2174754 | 0.91[ASN][1000 genomes] |
rs2305102 | 0.99[ASN][1000 genomes] |
rs2404773 | 0.91[ASN][1000 genomes] |
rs2660449 | 0.85[EUR][1000 genomes] |
rs2660454 | 0.84[EUR][1000 genomes] |
rs2660455 | 0.84[EUR][1000 genomes] |
rs2660459 | 0.83[EUR][1000 genomes] |
rs2708496 | 0.85[EUR][1000 genomes] |
rs2708498 | 0.84[EUR][1000 genomes] |
rs3765044 | 0.99[ASN][1000 genomes] |
rs4761074 | 0.99[ASN][1000 genomes] |
rs4761075 | 0.99[ASN][1000 genomes] |
rs4761115 | 0.97[ASN][1000 genomes] |
rs6539879 | 0.85[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6539881 | 0.96[EUR][1000 genomes] |
rs66617212 | 0.99[ASN][1000 genomes] |
rs7132596 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7133493 | 0.97[ASN][1000 genomes] |
rs7133817 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7302312 | 0.83[EUR][1000 genomes] |
rs7304576 | 0.99[ASN][1000 genomes] |
rs7312075 | 0.98[ASN][1000 genomes] |
rs7316900 | 0.96[EUR][1000 genomes] |
rs7954110 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7962577 | 0.99[EUR][1000 genomes] |
rs7965562 | 0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv899377 | chr12:85157346-85629241 | Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1040452 | chr12:85179586-85747907 | Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | esv1792335 | chr12:85321249-86003609 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:85402400-85408600 | Weak transcription | Hela-S3 | cervix |
2 | chr12:85402400-85409800 | Weak transcription | Muscle Satellite Cultured Cells | -- |
3 | chr12:85402400-85410200 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
4 | chr12:85403000-85409000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |