Variant report
Variant | rs74137407 |
---|---|
Chromosome Location | chr1:197857782-197857783 |
allele | A/G |
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:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000203724 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs55828314 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55873850 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57221255 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57319710 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs57805974 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs58603417 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs58959432 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59396394 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59498839 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60625077 | 1.00[AMR][1000 genomes] |
rs60873643 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60890417 | 1.00[AMR][1000 genomes] |
rs61374501 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134509 | 1.00[AMR][1000 genomes] |
rs74134865 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134866 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134867 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134869 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134870 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134873 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134874 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134877 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134878 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74137409 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999662 | chr1:197821769-197892803 | Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 14 gene(s) | inside rSNPs | diseases |
2 | esv2762214 | chr1:197821769-197897496 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive region | 14 gene(s) | inside rSNPs | diseases |
3 | nsv1004130 | chr1:197822757-197879728 | Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 13 gene(s) | inside rSNPs | diseases |
No data |