Variant report
Variant | rs1172927 |
---|---|
Chromosome Location | chr9:93492260-93492261 |
allele | 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 |
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No data |
rs_ID | r2[population] |
---|---|
rs1148844 | 0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1148846 | 0.80[AFR][1000 genomes] |
rs1172911 | 0.90[AFR][1000 genomes] |
rs1172912 | 0.90[AFR][1000 genomes] |
rs1172919 | 0.84[ASN][1000 genomes] |
rs1172920 | 0.81[ASN][1000 genomes] |
rs1172921 | 0.81[ASN][1000 genomes] |
rs1172924 | 0.89[ASN][1000 genomes] |
rs1172925 | 0.87[ASN][1000 genomes] |
rs1172929 | 0.88[AFR][1000 genomes] |
rs1172930 | 0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1173032 | 0.88[ASN][1000 genomes] |
rs1184620 | 0.86[AFR][1000 genomes] |
rs2126054 | 0.84[AFR][1000 genomes] |
rs2169237 | 0.84[AFR][1000 genomes] |
rs2613316 | 0.86[AFR][1000 genomes] |
rs2613326 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2810918 | 0.90[AFR][1000 genomes] |
rs2810919 | 0.81[ASN][1000 genomes] |
rs2810928 | 0.84[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1041278 | chr9:92965701-93560454 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1046989 | chr9:93353987-93800416 | Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv482757 | chr9:93356095-93543903 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:93490800-93499000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |