Variant report
Variant | rs12900070 |
---|---|
Chromosome Location | chr15:53184514-53184515 |
allele | C/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] |
---|---|
rs10851524 | 0.90[ASN][1000 genomes] |
rs11070921 | 0.95[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs11070935 | 0.80[EUR][1000 genomes] |
rs12912619 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12913472 | 0.84[EUR][1000 genomes] |
rs1899734 | 0.87[EUR][1000 genomes] |
rs1899736 | 0.88[ASN][1000 genomes] |
rs1899738 | 0.88[ASN][1000 genomes] |
rs1899739 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1899741 | 0.87[ASN][1000 genomes] |
rs2120447 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2165989 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2414185 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2414186 | 0.87[ASN][1000 genomes] |
rs4776079 | 0.87[ASN][1000 genomes] |
rs6493597 | 0.84[EUR][1000 genomes] |
rs6493598 | 0.84[EUR][1000 genomes] |
rs7166575 | 0.88[ASN][1000 genomes] |
rs8027796 | 0.88[ASN][1000 genomes] |
rs8030817 | 0.85[EUR][1000 genomes] |
rs8032241 | 0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs8032248 | 0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv471245 | chr15:52607262-53187165 | Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 52 gene(s) | inside rSNPs | diseases |
2 | nsv1043999 | chr15:53162917-53187508 | Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:53183600-53185600 | Weak transcription | Pancreas | Pancrea |