Variant report
Variant | rs11980883 |
---|---|
Chromosome Location | chr7:38747132-38747133 |
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)
No data |
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000006715 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10242807 | 0.91[ASN][1000 genomes] |
rs10243110 | 0.83[ASN][1000 genomes] |
rs10252285 | 0.93[ASN][1000 genomes] |
rs10262154 | 0.95[ASN][1000 genomes] |
rs10267709 | 0.88[ASN][1000 genomes] |
rs10277549 | 0.91[ASN][1000 genomes] |
rs10279367 | 0.95[ASN][1000 genomes] |
rs10281589 | 0.88[ASN][1000 genomes] |
rs11773094 | 0.95[ASN][1000 genomes] |
rs17617903 | 0.93[ASN][1000 genomes] |
rs17679853 | 0.93[ASN][1000 genomes] |
rs2286078 | 0.81[ASN][1000 genomes] |
rs2286107 | 0.93[ASN][1000 genomes] |
rs28520398 | 0.93[ASN][1000 genomes] |
rs28635894 | 0.84[ASN][1000 genomes] |
rs3779127 | 0.95[ASN][1000 genomes] |
rs3779128 | 0.93[ASN][1000 genomes] |
rs4610638 | 0.84[ASN][1000 genomes] |
rs55924838 | 0.98[ASN][1000 genomes] |
rs62444074 | 0.98[ASN][1000 genomes] |
rs6462863 | 0.81[ASN][1000 genomes] |
rs6956501 | 0.81[ASN][1000 genomes] |
rs6956969 | 0.83[ASN][1000 genomes] |
rs6973641 | 0.93[ASN][1000 genomes] |
rs7803132 | 0.95[ASN][1000 genomes] |
rs976353 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv887965 | chr7:38706384-38793243 | Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |