Variant report
Variant | rs9291303 |
---|---|
Chromosome Location | chr4:47108657-47108658 |
allele | C/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] |
---|---|
rs10011608 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs10025590 | 0.86[YRI][hapmap] |
rs10517179 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |
rs11730134 | 0.84[AFR][1000 genomes] |
rs12640095 | 0.88[YRI][hapmap] |
rs12645665 | 0.87[YRI][hapmap] |
rs1946966 | 0.81[YRI][hapmap] |
rs2351299 | 0.88[YRI][hapmap] |
rs28595484 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3775536 | 1.00[YRI][hapmap];0.91[AFR][1000 genomes] |
rs6854637 | 1.00[YRI][hapmap];0.91[AFR][1000 genomes] |
rs7663591 | 1.00[YRI][hapmap];0.91[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv537078 | chr4:47059778-47137372 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv829922 | chr4:47093785-47261181 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv879003 | chr4:47102993-47215939 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |