Variant report
Variant | rs55752923 |
---|---|
Chromosome Location | chr6:118367170-118367171 |
allele | A/G |
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] |
---|---|
rs12110607 | 1.00[EUR][1000 genomes] |
rs4132663 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4276535 | 1.00[EUR][1000 genomes] |
rs4307205 | 1.00[EUR][1000 genomes] |
rs4587199 | 1.00[EUR][1000 genomes] |
rs5003341 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56714111 | 1.00[AMR][1000 genomes] |
rs56993874 | 1.00[EUR][1000 genomes] |
rs58861108 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60541620 | 1.00[EUR][1000 genomes] |
rs61019727 | 1.00[EUR][1000 genomes] |
rs6568998 | 1.00[EUR][1000 genomes] |
rs6901514 | 1.00[EUR][1000 genomes] |
rs6935478 | 1.00[EUR][1000 genomes] |
rs73521541 | 1.00[EUR][1000 genomes] |
rs73525652 | 1.00[EUR][1000 genomes] |
rs73766425 | 1.00[EUR][1000 genomes] |
rs73766431 | 1.00[AMR][1000 genomes] |
rs73766467 | 1.00[AMR][1000 genomes] |
rs73768126 | 1.00[AMR][1000 genomes] |
rs73768145 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7775102 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7775110 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9385033 | 1.00[EUR][1000 genomes] |
rs9385034 | 1.00[EUR][1000 genomes] |
rs9387541 | 1.00[EUR][1000 genomes] |
rs9489309 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530526 | chr6:118027339-118718476 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:118365800-118375400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |