Variant report
Variant | rs12208740 |
---|---|
Chromosome Location | chr6:49985823-49985824 |
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)
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rs_ID | r2[population] |
---|---|
rs10948541 | 1.00[CEU][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12190383 | 0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12196609 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap] |
rs12197351 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs12197933 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs12208674 | 1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap] |
rs12213027 | 1.00[CEU][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes] |
rs6929062 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs6931140 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72864882 | 0.89[EUR][1000 genomes] |
rs7743362 | 0.88[EUR][1000 genomes] |
rs7759575 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv933942 | chr6:49480550-50004231 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
2 | nsv5295 | chr6:49955078-50007710 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |