Variant report
Variant | rs6693582 |
---|---|
Chromosome Location | chr1:225548126-225548127 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
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rs_ID | r2[population] |
---|---|
rs10495232 | 1.00[EUR][1000 genomes] |
rs10495235 | 1.00[EUR][1000 genomes] |
rs11805350 | 1.00[EUR][1000 genomes] |
rs12239042 | 1.00[YRI][hapmap] |
rs13376645 | 0.93[LWK][hapmap];1.00[MKK][hapmap];0.95[YRI][hapmap] |
rs1480102 | 1.00[EUR][1000 genomes] |
rs16844347 | 1.00[EUR][1000 genomes] |
rs16844357 | 1.00[EUR][1000 genomes] |
rs2153246 | 1.00[EUR][1000 genomes] |
rs56918103 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6664529 | 1.00[EUR][1000 genomes] |
rs6675157 | 1.00[EUR][1000 genomes] |
rs6675162 | 1.00[EUR][1000 genomes] |
rs6699883 | 1.00[EUR][1000 genomes] |
rs73136911 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73136918 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7512125 | 1.00[EUR][1000 genomes] |
rs7519130 | 1.00[EUR][1000 genomes] |
rs7536912 | 1.00[EUR][1000 genomes] |
rs7551251 | 1.00[EUR][1000 genomes] |
rs769297 | 1.00[EUR][1000 genomes] |
rs9803691 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv945672 | chr1:225339532-225561349 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv873226 | chr1:225347689-225555602 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:225547600-225548600 | Enhancers | Liver | Liver |