Variant report
Variant | rs7069875 |
---|---|
Chromosome Location | chr10:83123867-83123868 |
allele | A/G |
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] |
---|---|
rs10786402 | 0.93[ASN][1000 genomes] |
rs10883052 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11189512 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11189514 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12414363 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12415616 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2346229 | 0.93[ASN][1000 genomes] |
rs2493563 | 0.94[ASN][1000 genomes] |
rs473372 | 0.92[ASN][1000 genomes] |
rs500829 | 0.95[ASN][1000 genomes] |
rs510598 | 0.87[ASN][1000 genomes] |
rs511460 | 0.87[ASN][1000 genomes] |
rs528028 | 0.94[ASN][1000 genomes] |
rs528993 | 0.94[ASN][1000 genomes] |
rs529856 | 0.94[ASN][1000 genomes] |
rs552977 | 0.93[ASN][1000 genomes] |
rs553804 | 0.93[ASN][1000 genomes] |
rs555750 | 0.94[ASN][1000 genomes] |
rs557354 | 0.94[ASN][1000 genomes] |
rs561182 | 0.94[ASN][1000 genomes] |
rs586063 | 0.93[ASN][1000 genomes] |
rs587438 | 0.94[ASN][1000 genomes] |
rs632593 | 0.85[ASN][1000 genomes] |
rs633066 | 0.87[ASN][1000 genomes] |
rs649207 | 0.94[ASN][1000 genomes] |
rs681379 | 0.94[ASN][1000 genomes] |
rs681434 | 0.94[ASN][1000 genomes] |
rs7088454 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs751565 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs913633 | 0.94[ASN][1000 genomes] |
rs913634 | 0.94[ASN][1000 genomes] |
rs9420663 | 0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3449683 | chr10:82972143-83304804 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | esv3421917 | chr10:82972163-83304774 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv870428 | chr10:83035110-83306265 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv527269 | chr10:83119210-83134434 | Flanking Active TSS Enhancers Weak transcription | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:83123000-83126600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |