Variant report
Variant | rs28654762 |
---|---|
Chromosome Location | chr12:44596317-44596318 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10161163 | 1.00[ASN][1000 genomes] |
rs10161301 | 1.00[ASN][1000 genomes] |
rs10506233 | 1.00[ASN][1000 genomes] |
rs11182363 | 1.00[ASN][1000 genomes] |
rs11182371 | 1.00[ASN][1000 genomes] |
rs11182376 | 1.00[ASN][1000 genomes] |
rs11182389 | 1.00[ASN][1000 genomes] |
rs11182401 | 1.00[ASN][1000 genomes] |
rs12099550 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12296329 | 1.00[EUR][1000 genomes] |
rs12296939 | 1.00[ASN][1000 genomes] |
rs12302578 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12303163 | 1.00[ASN][1000 genomes] |
rs12303870 | 1.00[ASN][1000 genomes] |
rs12304783 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12306873 | 1.00[EUR][1000 genomes] |
rs12308508 | 0.87[ASN][1000 genomes] |
rs12308564 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12308750 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12309408 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12310801 | 1.00[ASN][1000 genomes] |
rs12311153 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12319385 | 1.00[ASN][1000 genomes] |
rs12319439 | 1.00[ASN][1000 genomes] |
rs12319776 | 1.00[ASN][1000 genomes] |
rs12320155 | 1.00[ASN][1000 genomes] |
rs12321149 | 1.00[ASN][1000 genomes] |
rs12321287 | 1.00[ASN][1000 genomes] |
rs1388775 | 1.00[ASN][1000 genomes] |
rs17094016 | 1.00[ASN][1000 genomes] |
rs17094227 | 0.83[EUR][1000 genomes] |
rs28538835 | 0.87[ASN][1000 genomes] |
rs57462004 | 1.00[ASN][1000 genomes] |
rs58851540 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59152420 | 0.87[ASN][1000 genomes] |
rs66993609 | 1.00[ASN][1000 genomes] |
rs73100825 | 0.87[ASN][1000 genomes] |
rs73100834 | 0.87[ASN][1000 genomes] |
rs73286295 | 0.83[EUR][1000 genomes] |
rs73286296 | 0.83[EUR][1000 genomes] |
rs73286301 | 0.83[EUR][1000 genomes] |
rs73288025 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288036 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288054 | 1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288073 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288075 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288080 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288085 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288089 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73288095 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290203 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290206 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290208 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290213 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290217 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290223 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290224 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290225 | 1.00[ASN][1000 genomes] |
rs73290228 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73290230 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs963095 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1049818 | chr12:44486312-45133783 | Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv832393 | chr12:44529406-44692414 | Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:44511400-44605800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |