Variant report
Variant | rs448075 |
---|---|
Chromosome Location | chr10:55338875-55338876 |
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] |
---|---|
rs10159501 | 0.81[EUR][1000 genomes] |
rs10762996 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12256830 | 0.89[ASN][1000 genomes] |
rs1387655 | 0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1387659 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1489843 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1932010 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1932011 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2050381 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2891482 | 0.89[ASN][1000 genomes] |
rs383804 | 0.90[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs386136 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs426872 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4271302 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs439136 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4935452 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs56105712 | 0.89[ASN][1000 genomes] |
rs6481024 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs66643903 | 0.89[ASN][1000 genomes] |
rs7098418 | 0.80[EUR][1000 genomes] |
rs72791375 | 0.89[ASN][1000 genomes] |
rs72791377 | 0.89[ASN][1000 genomes] |
rs72791378 | 0.83[ASN][1000 genomes] |
rs72791380 | 0.89[ASN][1000 genomes] |
rs72791385 | 0.83[ASN][1000 genomes] |
rs72791386 | 0.89[ASN][1000 genomes] |
rs72791387 | 0.89[ASN][1000 genomes] |
rs72791390 | 0.89[ASN][1000 genomes] |
rs72791393 | 0.89[ASN][1000 genomes] |
rs72791394 | 0.89[ASN][1000 genomes] |
rs72793106 | 0.89[ASN][1000 genomes] |
rs72793107 | 0.89[ASN][1000 genomes] |
rs7904493 | 0.87[EUR][1000 genomes] |
rs9416277 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs9416285 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752952 | chr10:54900994-55497594 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1044282 | chr10:55186501-55516392 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv540631 | chr10:55186501-55516392 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1043501 | chr10:55186701-55516253 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv540632 | chr10:55186701-55516253 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv1050323 | chr10:55190079-55546575 | Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:55338000-55339800 | Enhancers | Fetal Lung | lung |
2 | chr10:55338400-55339400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
3 | chr10:55338600-55339000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
4 | chr10:55338600-55339400 | Enhancers | HUVEC | blood vessel |