Variant report
Variant | rs7754093 |
---|---|
Chromosome Location | chr6:139989746-139989747 |
allele | A/G |
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)
No data |
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000164442 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs55689234 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55755046 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55961359 | 1.00[EUR][1000 genomes] |
rs56245861 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56335309 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59731656 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61478054 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61657098 | 0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61693276 | 0.80[EUR][1000 genomes] |
rs73556057 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7743179 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7756228 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9495558 | 1.00[EUR][1000 genomes] |
rs9495560 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9495562 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869066 | chr6:139777114-140639695 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 26 gene(s) | inside rSNPs | diseases |
2 | nsv516840 | chr6:139960833-140053704 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |