Variant report
Variant | rs4550099 |
---|---|
Chromosome Location | chr1:56747083-56747084 |
allele | C/T |
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] |
---|---|
rs10789017 | 0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10888964 | 0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs11206772 | 0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs1581994 | 0.90[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs2096086 | 0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2105301 | 0.80[AFR][1000 genomes] |
rs2777758 | 0.83[EUR][1000 genomes] |
rs2792774 | 0.81[EUR][1000 genomes] |
rs2792775 | 0.81[EUR][1000 genomes] |
rs2792776 | 0.81[EUR][1000 genomes] |
rs2793663 | 0.86[EUR][1000 genomes] |
rs2793665 | 0.86[EUR][1000 genomes] |
rs2793666 | 0.86[EUR][1000 genomes] |
rs2793691 | 0.81[EUR][1000 genomes] |
rs61773389 | 0.80[EUR][1000 genomes] |
rs6588616 | 0.82[AMR][1000 genomes] |
rs7417415 | 0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs9436537 | 0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9787032 | 0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs9787033 | 0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1006422 | chr1:56734772-56828606 | Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
2 | nsv534972 | chr1:56734772-56828606 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:56745400-56757000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |