Variant report
Variant | rs11013473 |
---|---|
Chromosome Location | chr10:23718860-23718861 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs11013468 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11013469 | 0.91[EUR][1000 genomes] |
rs11013474 | 0.87[ASN][1000 genomes] |
rs11013475 | 0.91[EUR][1000 genomes] |
rs11013476 | 0.85[ASN][1000 genomes] |
rs11013478 | 0.87[ASN][1000 genomes] |
rs11013479 | 0.99[ASN][1000 genomes] |
rs11013480 | 0.87[ASN][1000 genomes] |
rs11013481 | 0.87[ASN][1000 genomes] |
rs11013482 | 0.98[ASN][1000 genomes] |
rs11013483 | 0.97[ASN][1000 genomes] |
rs11013484 | 0.84[ASN][1000 genomes] |
rs11013486 | 0.91[EUR][1000 genomes] |
rs11013488 | 0.91[EUR][1000 genomes] |
rs11013490 | 0.91[EUR][1000 genomes] |
rs11013491 | 0.80[ASN][1000 genomes] |
rs11013501 | 0.91[EUR][1000 genomes] |
rs12246797 | 0.91[EUR][1000 genomes] |
rs12254101 | 1.00[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs12254124 | 0.91[EUR][1000 genomes] |
rs12258295 | 0.91[EUR][1000 genomes] |
rs12265309 | 0.91[EUR][1000 genomes] |
rs12266879 | 0.91[EUR][1000 genomes] |
rs12571102 | 0.94[ASN][1000 genomes] |
rs12571351 | 0.82[ASN][1000 genomes] |
rs12571384 | 0.97[ASN][1000 genomes] |
rs12572169 | 0.97[ASN][1000 genomes] |
rs1398026 | 0.91[EUR][1000 genomes] |
rs1511825 | 0.91[EUR][1000 genomes] |
rs1553905 | 1.00[ASN][1000 genomes] |
rs16923233 | 0.87[ASN][1000 genomes] |
rs16923259 | 0.80[ASN][1000 genomes] |
rs1995981 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2089876 | 0.96[ASN][1000 genomes] |
rs2089878 | 0.89[ASN][1000 genomes] |
rs2089879 | 0.97[ASN][1000 genomes] |
rs2089880 | 0.94[ASN][1000 genomes] |
rs35182895 | 0.89[ASN][1000 genomes] |
rs3934842 | 0.91[EUR][1000 genomes] |
rs4442437 | 0.99[ASN][1000 genomes] |
rs4747470 | 0.98[ASN][1000 genomes] |
rs4747471 | 0.86[ASN][1000 genomes] |
rs4747474 | 1.00[ASN][1000 genomes] |
rs4748885 | 1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4748886 | 0.99[ASN][1000 genomes] |
rs4748887 | 0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4748889 | 0.87[ASN][1000 genomes] |
rs57566783 | 0.99[ASN][1000 genomes] |
rs58056630 | 0.97[ASN][1000 genomes] |
rs58305149 | 0.85[ASN][1000 genomes] |
rs58604095 | 0.99[ASN][1000 genomes] |
rs58614955 | 0.87[ASN][1000 genomes] |
rs59547906 | 0.87[ASN][1000 genomes] |
rs6482276 | 0.99[ASN][1000 genomes] |
rs7072045 | 0.91[EUR][1000 genomes] |
rs7079490 | 0.94[ASN][1000 genomes] |
rs7079866 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7080648 | 0.91[EUR][1000 genomes] |
rs7080700 | 0.99[ASN][1000 genomes] |
rs7083306 | 0.93[ASN][1000 genomes] |
rs7084145 | 0.91[EUR][1000 genomes] |
rs7084431 | 0.98[ASN][1000 genomes] |
rs7084695 | 0.91[EUR][1000 genomes] |
rs7087230 | 0.99[ASN][1000 genomes] |
rs7092162 | 0.90[ASN][1000 genomes] |
rs7094796 | 0.91[EUR][1000 genomes] |
rs7096353 | 0.99[ASN][1000 genomes] |
rs7097072 | 0.99[ASN][1000 genomes] |
rs7097167 | 0.91[EUR][1000 genomes] |
rs7097185 | 0.91[EUR][1000 genomes] |
rs7098076 | 0.99[ASN][1000 genomes] |
rs7100463 | 0.99[ASN][1000 genomes] |
rs7100518 | 0.99[ASN][1000 genomes] |
rs73602555 | 0.88[ASN][1000 genomes] |
rs73602556 | 0.96[ASN][1000 genomes] |
rs74122431 | 0.87[ASN][1000 genomes] |
rs74122432 | 0.87[ASN][1000 genomes] |
rs74122435 | 0.87[ASN][1000 genomes] |
rs74122436 | 0.87[ASN][1000 genomes] |
rs74122437 | 0.87[ASN][1000 genomes] |
rs7905070 | 1.00[EUR][1000 genomes] |
rs7919581 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv825305 | chr10:23698620-23740919 | Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:23712000-23719000 | Weak transcription | Stomach Mucosa | stomach |