Variant report
Variant | rs1485940 |
---|---|
Chromosome Location | chr4:175648164-175648165 |
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] |
---|---|
rs10000984 | 0.83[YRI][hapmap] |
rs10007273 | 1.00[CEU][hapmap];0.85[YRI][hapmap] |
rs10009999 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs10520290 | 0.80[ASN][1000 genomes] |
rs11725853 | 0.83[ASN][1000 genomes] |
rs12499257 | 0.81[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs1485939 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs1485941 | 1.00[CEU][hapmap];0.80[YRI][hapmap] |
rs1586338 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs17060785 | 0.80[ASN][1000 genomes] |
rs2877828 | 0.80[ASN][1000 genomes] |
rs4447833 | 0.80[ASN][1000 genomes] |
rs4594702 | 0.82[ASN][1000 genomes] |
rs7656851 | 0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs7658547 | 0.85[YRI][hapmap];0.81[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs7685854 | 0.82[ASN][1000 genomes] |
rs9312559 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869116 | chr4:175231090-175801761 | Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv1018390 | chr4:175475505-175969742 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
No data |