Variant report
Variant | rs60823467 |
---|---|
Chromosome Location | chr11:71924434-71924435 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
1
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
FOLR2 | TF binding region |
ENSG00000204971 | TF binding region |
ENSG00000204971 | Chromatin interaction |
ENSG00000165458 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10501409 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11235467 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11235468 | 0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs12809011 | 0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs34468529 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs34897504 | 0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs35805771 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs66484462 | 0.90[ASN][1000 genomes] |
rs68068983 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs71477716 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530623 | chr11:71088949-72020418 | Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 134 gene(s) | inside rSNPs | diseases |
No data |