Variant report
Variant | rs9455370 |
---|---|
Chromosome Location | chr6:71881214-71881215 |
allele | A/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] |
---|---|
rs1013408 | 1.00[ASN][1000 genomes] |
rs10806642 | 1.00[ASN][1000 genomes] |
rs10806645 | 1.00[ASN][1000 genomes] |
rs10806646 | 1.00[ASN][1000 genomes] |
rs10945289 | 1.00[ASN][1000 genomes] |
rs10945293 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11967291 | 1.00[ASN][1000 genomes] |
rs12055466 | 1.00[ASN][1000 genomes] |
rs12055852 | 1.00[ASN][1000 genomes] |
rs12110395 | 1.00[ASN][1000 genomes] |
rs12205990 | 1.00[ASN][1000 genomes] |
rs1418679 | 1.00[ASN][1000 genomes] |
rs1418680 | 1.00[ASN][1000 genomes] |
rs1418681 | 1.00[ASN][1000 genomes] |
rs1418683 | 1.00[ASN][1000 genomes] |
rs1539424 | 1.00[ASN][1000 genomes] |
rs1539425 | 1.00[ASN][1000 genomes] |
rs1539426 | 1.00[ASN][1000 genomes] |
rs1739801 | 1.00[ASN][1000 genomes] |
rs1739805 | 1.00[ASN][1000 genomes] |
rs1739808 | 1.00[ASN][1000 genomes] |
rs1775549 | 1.00[ASN][1000 genomes] |
rs1832948 | 1.00[ASN][1000 genomes] |
rs1832949 | 1.00[ASN][1000 genomes] |
rs1857218 | 1.00[ASN][1000 genomes] |
rs1935792 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1935793 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1935796 | 1.00[ASN][1000 genomes] |
rs1935797 | 1.00[ASN][1000 genomes] |
rs1935798 | 1.00[ASN][1000 genomes] |
rs1935799 | 1.00[ASN][1000 genomes] |
rs2096216 | 1.00[ASN][1000 genomes] |
rs2096217 | 1.00[ASN][1000 genomes] |
rs2153912 | 1.00[ASN][1000 genomes] |
rs2207677 | 1.00[ASN][1000 genomes] |
rs2347922 | 1.00[ASN][1000 genomes] |
rs4434432 | 1.00[ASN][1000 genomes] |
rs4707897 | 1.00[ASN][1000 genomes] |
rs4707898 | 1.00[ASN][1000 genomes] |
rs57458638 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57813102 | 1.00[AFR][1000 genomes] |
rs58391752 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60360675 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61020445 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6455408 | 1.00[ASN][1000 genomes] |
rs6455409 | 1.00[ASN][1000 genomes] |
rs6899313 | 1.00[ASN][1000 genomes] |
rs6899520 | 1.00[ASN][1000 genomes] |
rs6914378 | 1.00[ASN][1000 genomes] |
rs6937195 | 1.00[ASN][1000 genomes] |
rs6941623 | 1.00[ASN][1000 genomes] |
rs72926558 | 1.00[ASN][1000 genomes] |
rs73502802 | 1.00[ASN][1000 genomes] |
rs73746998 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73747002 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7739792 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9342811 | 1.00[ASN][1000 genomes] |
rs9342813 | 1.00[ASN][1000 genomes] |
rs9342814 | 1.00[ASN][1000 genomes] |
rs9346438 | 1.00[ASN][1000 genomes] |
rs9351802 | 1.00[ASN][1000 genomes] |
rs9354961 | 1.00[ASN][1000 genomes] |
rs9360439 | 1.00[ASN][1000 genomes] |
rs9364135 | 1.00[ASN][1000 genomes] |
rs9446350 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9446351 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9455335 | 1.00[ASN][1000 genomes] |
rs9455336 | 1.00[ASN][1000 genomes] |
rs9455364 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv527265 | chr6:71867477-71902656 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv886149 | chr6:71875777-71936292 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:71880400-71881400 | Enhancers | Fetal Intestine Small | intestine |
2 | chr6:71880600-71881800 | Enhancers | Fetal Intestine Large | intestine |