Variant report
Variant | rs7067635 |
---|---|
Chromosome Location | chr10:23805013-23805014 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:23793550..23795585-chr10:23803256..23805113,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10828460 | 1.00[EUR][1000 genomes] |
rs10828461 | 1.00[EUR][1000 genomes] |
rs10828473 | 1.00[EUR][1000 genomes] |
rs11013472 | 1.00[EUR][1000 genomes] |
rs11013474 | 1.00[EUR][1000 genomes] |
rs11013476 | 1.00[EUR][1000 genomes] |
rs11013478 | 1.00[EUR][1000 genomes] |
rs11013479 | 0.89[CHB][hapmap];1.00[EUR][1000 genomes] |
rs11013480 | 1.00[EUR][1000 genomes] |
rs11013481 | 1.00[EUR][1000 genomes] |
rs11013482 | 1.00[EUR][1000 genomes] |
rs11013483 | 1.00[EUR][1000 genomes] |
rs11013484 | 1.00[EUR][1000 genomes] |
rs11013491 | 1.00[EUR][1000 genomes] |
rs11013492 | 1.00[EUR][1000 genomes] |
rs11013494 | 1.00[EUR][1000 genomes] |
rs11013495 | 1.00[EUR][1000 genomes] |
rs11013496 | 1.00[EUR][1000 genomes] |
rs11013497 | 1.00[EUR][1000 genomes] |
rs11013498 | 1.00[EUR][1000 genomes] |
rs11013527 | 1.00[EUR][1000 genomes] |
rs11013539 | 1.00[EUR][1000 genomes] |
rs11013544 | 1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11013558 | 1.00[EUR][1000 genomes] |
rs11013561 | 1.00[EUR][1000 genomes] |
rs11527594 | 1.00[EUR][1000 genomes] |
rs12217320 | 1.00[EUR][1000 genomes] |
rs12219829 | 1.00[EUR][1000 genomes] |
rs12569512 | 1.00[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12571102 | 1.00[EUR][1000 genomes] |
rs12571351 | 1.00[EUR][1000 genomes] |
rs12571384 | 1.00[EUR][1000 genomes] |
rs12572169 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs1398027 | 1.00[EUR][1000 genomes] |
rs1553905 | 1.00[EUR][1000 genomes] |
rs16923233 | 1.00[EUR][1000 genomes] |
rs16923259 | 1.00[EUR][1000 genomes] |
rs16923277 | 1.00[EUR][1000 genomes] |
rs2089876 | 1.00[EUR][1000 genomes] |
rs2089878 | 1.00[EUR][1000 genomes] |
rs2089879 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs2089880 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs3898626 | 1.00[EUR][1000 genomes] |
rs4442437 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs4747470 | 1.00[EUR][1000 genomes] |
rs4747471 | 1.00[EUR][1000 genomes] |
rs4747474 | 1.00[EUR][1000 genomes] |
rs4747475 | 1.00[EUR][1000 genomes] |
rs4747476 | 1.00[EUR][1000 genomes] |
rs4748886 | 1.00[EUR][1000 genomes] |
rs4748889 | 1.00[EUR][1000 genomes] |
rs4748891 | 1.00[EUR][1000 genomes] |
rs4748895 | 1.00[EUR][1000 genomes] |
rs4748904 | 1.00[EUR][1000 genomes] |
rs57566783 | 1.00[EUR][1000 genomes] |
rs58056630 | 1.00[EUR][1000 genomes] |
rs58305149 | 1.00[EUR][1000 genomes] |
rs58604095 | 1.00[EUR][1000 genomes] |
rs58614955 | 1.00[EUR][1000 genomes] |
rs59547906 | 1.00[EUR][1000 genomes] |
rs61412542 | 1.00[EUR][1000 genomes] |
rs6482276 | 1.00[EUR][1000 genomes] |
rs7079349 | 0.91[CHB][hapmap] |
rs7079490 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7080700 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7083306 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7084431 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7087230 | 1.00[EUR][1000 genomes] |
rs7096353 | 0.91[CHB][hapmap] |
rs7097072 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7098076 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7100463 | 1.00[EUR][1000 genomes] |
rs7100518 | 1.00[EUR][1000 genomes] |
rs73602555 | 1.00[EUR][1000 genomes] |
rs73602556 | 1.00[EUR][1000 genomes] |
rs74122431 | 1.00[EUR][1000 genomes] |
rs74122432 | 1.00[EUR][1000 genomes] |
rs74122435 | 1.00[EUR][1000 genomes] |
rs74122436 | 1.00[EUR][1000 genomes] |
rs7919581 | 0.91[CHB][hapmap];1.00[EUR][1000 genomes] |
rs867892 | 1.00[EUR][1000 genomes] |
rs945778 | 1.00[EUR][1000 genomes] |
rs9633627 | 1.00[EUR][1000 genomes] |
rs9633648 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831811 | chr10:23734326-23913370 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv466835 | chr10:23801555-23869175 | Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
3 | nsv550215 | chr10:23801555-23869175 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
4 | esv2761580 | chr10:23804215-23806382 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:23803800-23805600 | Enhancers | Hela-S3 | cervix |