Variant report
Variant | rs7074552 |
---|---|
Chromosome Location | chr10:116909988-116909989 |
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] |
---|---|
rs10749173 | 1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10787565 | 1.00[CEU][hapmap] |
rs10885679 | 1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs11197158 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs1264747 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs1268915 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs1856357 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs1953758 | 1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs2201364 | 0.85[AMR][1000 genomes] |
rs2255916 | 0.85[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2264063 | 1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2265929 | 1.00[CEU][hapmap] |
rs2492983 | 0.89[EUR][1000 genomes] |
rs41314493 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4409743 | 1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs4752730 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs57236143 | 0.89[EUR][1000 genomes] |
rs6585323 | 1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7099807 | 0.89[EUR][1000 genomes] |
rs7915481 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3435429 | chr10:116394152-117006347 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv831998 | chr10:116847998-116969618 | Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv869279 | chr10:116884639-117032437 | Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |