Variant report
Variant | rs4502809 |
---|---|
Chromosome Location | chr5:147311972-147311973 |
allele | A/C |
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] |
---|---|
rs10036463 | 1.00[EUR][1000 genomes] |
rs10037068 | 0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10037369 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10037673 | 1.00[EUR][1000 genomes] |
rs10038266 | 1.00[EUR][1000 genomes] |
rs10038968 | 1.00[EUR][1000 genomes] |
rs10041966 | 1.00[EUR][1000 genomes] |
rs10042754 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10044155 | 1.00[EUR][1000 genomes] |
rs10052920 | 1.00[EUR][1000 genomes] |
rs10054271 | 0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10055303 | 1.00[EUR][1000 genomes] |
rs10056793 | 1.00[EUR][1000 genomes] |
rs10057434 | 1.00[EUR][1000 genomes] |
rs10060456 | 1.00[EUR][1000 genomes] |
rs10063124 | 1.00[EUR][1000 genomes] |
rs10063154 | 1.00[EUR][1000 genomes] |
rs10064440 | 1.00[EUR][1000 genomes] |
rs10065895 | 1.00[EUR][1000 genomes] |
rs10067543 | 1.00[EUR][1000 genomes] |
rs10067929 | 1.00[EUR][1000 genomes] |
rs10069389 | 1.00[EUR][1000 genomes] |
rs10070673 | 1.00[EUR][1000 genomes] |
rs10072814 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10074421 | 1.00[EUR][1000 genomes] |
rs10075087 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10075879 | 1.00[EUR][1000 genomes] |
rs10076722 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10076759 | 1.00[EUR][1000 genomes] |
rs10077349 | 1.00[EUR][1000 genomes] |
rs10078401 | 1.00[EUR][1000 genomes] |
rs10079585 | 1.00[EUR][1000 genomes] |
rs10079907 | 1.00[EUR][1000 genomes] |
rs10477356 | 1.00[EUR][1000 genomes] |
rs10477361 | 1.00[EUR][1000 genomes] |
rs10477362 | 1.00[EUR][1000 genomes] |
rs10515598 | 1.00[EUR][1000 genomes] |
rs10515604 | 1.00[EUR][1000 genomes] |
rs11952390 | 0.94[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11956316 | 1.00[EUR][1000 genomes] |
rs11960859 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13357089 | 1.00[EUR][1000 genomes] |
rs13436290 | 1.00[EUR][1000 genomes] |
rs13436617 | 1.00[EUR][1000 genomes] |
rs13436756 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13436799 | 1.00[EUR][1000 genomes] |
rs13436800 | 1.00[EUR][1000 genomes] |
rs1422984 | 1.00[EUR][1000 genomes] |
rs17096677 | 1.00[EUR][1000 genomes] |
rs17107495 | 1.00[EUR][1000 genomes] |
rs17107570 | 1.00[EUR][1000 genomes] |
rs17107730 | 1.00[EUR][1000 genomes] |
rs17107741 | 1.00[EUR][1000 genomes] |
rs28433470 | 1.00[EUR][1000 genomes] |
rs28449960 | 1.00[EUR][1000 genomes] |
rs28545137 | 1.00[EUR][1000 genomes] |
rs28573919 | 1.00[EUR][1000 genomes] |
rs28631785 | 1.00[EUR][1000 genomes] |
rs28732977 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28753859 | 1.00[EUR][1000 genomes] |
rs4529179 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4994723 | 1.00[EUR][1000 genomes] |
rs56121007 | 1.00[EUR][1000 genomes] |
rs57186409 | 1.00[EUR][1000 genomes] |
rs57804951 | 1.00[EUR][1000 genomes] |
rs58069263 | 1.00[EUR][1000 genomes] |
rs58257443 | 1.00[EUR][1000 genomes] |
rs60076377 | 1.00[EUR][1000 genomes] |
rs60206159 | 1.00[EUR][1000 genomes] |
rs60937504 | 1.00[EUR][1000 genomes] |
rs61331507 | 1.00[EUR][1000 genomes] |
rs73265206 | 1.00[EUR][1000 genomes] |
rs73265249 | 1.00[EUR][1000 genomes] |
rs73265266 | 1.00[EUR][1000 genomes] |
rs73265280 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73265300 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73265302 | 1.00[EUR][1000 genomes] |
rs73271118 | 1.00[EUR][1000 genomes] |
rs73794605 | 1.00[EUR][1000 genomes] |
rs73797307 | 1.00[EUR][1000 genomes] |
rs73797311 | 1.00[EUR][1000 genomes] |
rs7700644 | 1.00[EUR][1000 genomes] |
rs9325051 | 1.00[EUR][1000 genomes] |
rs9325053 | 1.00[EUR][1000 genomes] |
rs9325054 | 1.00[EUR][1000 genomes] |
rs9325055 | 1.00[EUR][1000 genomes] |
rs9325056 | 1.00[EUR][1000 genomes] |
rs9325059 | 1.00[EUR][1000 genomes] |
rs9325060 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3334831 | chr5:147165950-147339765 | Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv1028477 | chr5:147255013-147416217 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:147307200-147314200 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr5:147308200-147312200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
3 | chr5:147311200-147312200 | Enhancers | Fetal Heart | heart |
4 | chr5:147311400-147312200 | Enhancers | Esophagus | oesophagus |
5 | chr5:147311800-147313200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |