Variant report
Variant | rs9841084 |
---|---|
Chromosome Location | chr3:94491288-94491289 |
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 |
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No data |
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No data |
rs_ID | r2[population] |
---|---|
rs13314320 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13324772 | 0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13324801 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1368197 | 0.84[AMR][1000 genomes] |
rs1368198 | 0.83[AMR][1000 genomes] |
rs1368199 | 0.80[AMR][1000 genomes] |
rs2163680 | 0.80[AMR][1000 genomes] |
rs2163682 | 0.80[AMR][1000 genomes] |
rs4241479 | 0.81[AMR][1000 genomes] |
rs4462967 | 0.87[ASN][1000 genomes] |
rs4493433 | 0.84[AMR][1000 genomes] |
rs4583664 | 0.82[AMR][1000 genomes] |
rs6780216 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7427844 | 0.81[AMR][1000 genomes] |
rs7642399 | 0.84[AMR][1000 genomes] |
rs7646332 | 0.84[AMR][1000 genomes] |
rs7652148 | 0.84[AMR][1000 genomes] |
rs7653317 | 0.84[AMR][1000 genomes] |
rs7653599 | 0.84[AMR][1000 genomes] |
rs9637418 | 0.84[AMR][1000 genomes] |
rs9814299 | 0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9832016 | 0.82[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs9832891 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9842192 | 0.86[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs9842195 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs9842368 | 0.86[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs9847887 | 0.84[AMR][1000 genomes] |
rs9848372 | 0.83[AMR][1000 genomes] |
rs9867704 | 0.82[AMR][1000 genomes] |
rs9872890 | 0.84[AMR][1000 genomes] |
rs9879048 | 0.84[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869241 | chr3:93527675-94504491 | Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
2 | nsv1004176 | chr3:93654100-94502551 | Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
3 | nsv460763 | chr3:94384332-94596072 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv590988 | chr3:94384332-94596072 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv877167 | chr3:94430430-94554720 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv877168 | chr3:94430430-94614333 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv460764 | chr3:94479849-94654181 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
8 | nsv590989 | chr3:94479849-94654181 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | TF binding regionChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
9 | esv1803616 | chr3:94487032-94538580 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:94491200-94491800 | Enhancers | Rectal Mucosa Donor 31 | rectum |