Variant report
Variant | rs57848797 |
---|---|
Chromosome Location | chr9:116627146-116627147 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000157657 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10817523 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10981940 | 0.94[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs10981982 | 0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10981988 | 0.82[AMR][1000 genomes] |
rs10981990 | 0.82[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs12551439 | 0.81[AMR][1000 genomes] |
rs12551482 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs16910261 | 0.82[AMR][1000 genomes] |
rs2418253 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs35929232 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56730168 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60668360 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61533724 | 0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7020963 | 0.94[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7852347 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv430093 | chr9:116330446-117325446 | Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 165 gene(s) | inside rSNPs | diseases |
No data |