Variant report
Variant | rs1561115 |
---|---|
Chromosome Location | chr3:25260453-25260454 |
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] |
---|---|
rs10510558 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10510559 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10510560 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs10510561 | 0.96[EUR][1000 genomes] |
rs13068143 | 0.94[EUR][1000 genomes] |
rs13068891 | 0.85[CEU][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap] |
rs13074533 | 0.94[EUR][1000 genomes] |
rs13082318 | 0.94[EUR][1000 genomes] |
rs13085280 | 0.96[EUR][1000 genomes] |
rs13087573 | 0.96[EUR][1000 genomes] |
rs13087919 | 0.86[EUR][1000 genomes] |
rs13088581 | 0.99[EUR][1000 genomes] |
rs13090740 | 0.96[EUR][1000 genomes] |
rs13092896 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13093059 | 0.96[EUR][1000 genomes] |
rs13096074 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1436239 | 0.85[EUR][1000 genomes] |
rs1601161 | 0.96[EUR][1000 genomes] |
rs1601162 | 0.96[EUR][1000 genomes] |
rs17015971 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17015978 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17016060 | 0.95[EUR][1000 genomes] |
rs17016078 | 0.96[EUR][1000 genomes] |
rs17016133 | 0.93[EUR][1000 genomes] |
rs17578259 | 0.86[EUR][1000 genomes] |
rs1992059 | 0.94[EUR][1000 genomes] |
rs1992060 | 0.98[EUR][1000 genomes] |
rs34197182 | 0.83[EUR][1000 genomes] |
rs34403304 | 0.98[EUR][1000 genomes] |
rs34537630 | 0.96[EUR][1000 genomes] |
rs34820979 | 0.93[EUR][1000 genomes] |
rs34985047 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs35180299 | 0.93[EUR][1000 genomes] |
rs35264689 | 0.89[EUR][1000 genomes] |
rs35336027 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs35508620 | 0.94[EUR][1000 genomes] |
rs35646412 | 0.95[EUR][1000 genomes] |
rs35888700 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs56062751 | 0.87[EUR][1000 genomes] |
rs57402663 | 0.96[EUR][1000 genomes] |
rs61228958 | 0.96[EUR][1000 genomes] |
rs66807073 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs66939282 | 0.96[EUR][1000 genomes] |
rs67150539 | 0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs67681308 | 0.94[EUR][1000 genomes] |
rs6779499 | 0.97[EUR][1000 genomes] |
rs67880640 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs67912541 | 0.96[EUR][1000 genomes] |
rs6792184 | 0.97[EUR][1000 genomes] |
rs68073275 | 0.96[EUR][1000 genomes] |
rs73042375 | 0.91[EUR][1000 genomes] |
rs73042380 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs73044294 | 0.98[EUR][1000 genomes] |
rs73045965 | 0.98[EUR][1000 genomes] |
rs7427426 | 0.96[EUR][1000 genomes] |
rs7432016 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949035 | chr3:25194301-26084890 | Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 68 gene(s) | inside rSNPs | diseases |
2 | nsv508213 | chr3:25206150-25326196 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:25259600-25260600 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr3:25260200-25265600 | Weak transcription | Fetal Heart | heart |