Variant report
Variant | rs949715 |
---|---|
Chromosome Location | chr3:24126325-24126326 |
allele | A/C/G/T |
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] |
---|---|
rs11705746 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs11708328 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs11709111 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs11709760 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11714770 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs11714787 | 0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11718240 | 0.89[EUR][1000 genomes] |
rs11721182 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs17014081 | 0.86[EUR][1000 genomes] |
rs17014136 | 0.95[EUR][1000 genomes] |
rs1799888 | 0.90[ASN][1000 genomes] |
rs1868573 | 0.90[ASN][1000 genomes] |
rs2063481 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2089848 | 0.92[EUR][1000 genomes] |
rs2278802 | 0.84[EUR][1000 genomes] |
rs28503241 | 0.96[EUR][1000 genomes] |
rs28702740 | 0.96[EUR][1000 genomes] |
rs35316896 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6782978 | 0.93[ASN][1000 genomes] |
rs73822696 | 0.93[EUR][1000 genomes] |
rs7645692 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533980 | chr3:23445901-24311972 | ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 64 gene(s) | inside rSNPs | diseases |
2 | nsv834639 | chr3:24037113-24233925 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
3 | nsv1004037 | chr3:24064777-24143719 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:24119600-24128200 | Weak transcription | Aorta | Aorta |