Variant report
Variant | rs7778716 |
---|---|
Chromosome Location | chr7:127154121-127154122 |
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 |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000048405 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10085369 | 0.92[EUR][1000 genomes] |
rs10230430 | 0.92[EUR][1000 genomes] |
rs10237869 | 0.92[EUR][1000 genomes] |
rs10238433 | 0.80[EUR][1000 genomes] |
rs10258030 | 0.89[EUR][1000 genomes] |
rs10263237 | 0.80[EUR][1000 genomes] |
rs10267162 | 0.92[EUR][1000 genomes] |
rs10276292 | 0.89[EUR][1000 genomes] |
rs1107491 | 1.00[GIH][hapmap];0.85[MEX][hapmap];0.97[EUR][1000 genomes] |
rs11763731 | 0.92[EUR][1000 genomes] |
rs17151018 | 0.89[EUR][1000 genomes] |
rs28393048 | 0.97[EUR][1000 genomes] |
rs28807149 | 0.89[EUR][1000 genomes] |
rs56406547 | 0.86[EUR][1000 genomes] |
rs61667750 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6467139 | 0.89[EUR][1000 genomes] |
rs6973507 | 0.92[EUR][1000 genomes] |
rs6977152 | 0.89[EUR][1000 genomes] |
rs73459063 | 0.85[EUR][1000 genomes] |
rs73459083 | 0.89[EUR][1000 genomes] |
rs7777815 | 0.87[EUR][1000 genomes] |
rs7778682 | 1.00[YRI][hapmap];0.92[AFR][1000 genomes] |
rs7781622 | 0.80[EUR][1000 genomes] |
rs7784284 | 0.91[AFR][1000 genomes] |
rs7784533 | 0.89[EUR][1000 genomes] |
rs7811205 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831122 | chr7:127143207-127357885 | Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
No data |