Variant report
Variant | rs56394800 |
---|---|
Chromosome Location | chr8:60605208-60605209 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:60568709..60570705-chr8:60604991..60607479,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12334344 | 0.95[EUR][1000 genomes] |
rs12549153 | 0.89[EUR][1000 genomes] |
rs1588499 | 0.98[EUR][1000 genomes] |
rs16925109 | 1.00[AFR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs16925119 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs28590033 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4629854 | 0.89[EUR][1000 genomes] |
rs4644228 | 0.86[AFR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs55641496 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs57114745 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs60587092 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs62504703 | 0.94[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs62504733 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62506400 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs62506401 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs6651299 | 0.80[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72655599 | 0.98[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1030564 | chr8:60445016-60752655 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv539630 | chr8:60445016-60752655 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:60601800-60606200 | Weak transcription | Fetal Stomach | stomach |