Variant report
Variant | rs1703574 |
---|---|
Chromosome Location | chr8:50066050-50066051 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10957382 | 0.97[ASN][1000 genomes] |
rs13256466 | 0.97[ASN][1000 genomes] |
rs1383274 | 0.97[ASN][1000 genomes] |
rs1383276 | 0.97[ASN][1000 genomes] |
rs1383279 | 0.97[ASN][1000 genomes] |
rs1480388 | 0.97[ASN][1000 genomes] |
rs1480389 | 0.97[ASN][1000 genomes] |
rs1480390 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1585895 | 0.97[ASN][1000 genomes] |
rs1703573 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1842403 | 0.97[ASN][1000 genomes] |
rs1842404 | 0.90[ASN][1000 genomes] |
rs2891746 | 0.90[ASN][1000 genomes] |
rs4427188 | 0.97[ASN][1000 genomes] |
rs6985247 | 0.93[ASN][1000 genomes] |
rs7001422 | 0.97[ASN][1000 genomes] |
rs7015074 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73678572 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7832761 | 0.97[ASN][1000 genomes] |
rs9792367 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1025068 | chr8:49953397-50370208 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
2 | esv1793350 | chr8:50013702-50102628 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1034908 | chr8:50023423-50416049 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv539601 | chr8:50023423-50416049 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1024410 | chr8:50037085-50511501 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:50066000-50069000 | Weak transcription | GM12878-XiMat | blood |