Variant report
Variant | rs56218359 |
---|---|
Chromosome Location | chr9:104102383-104102384 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10114241 | 0.96[ASN][1000 genomes] |
rs10120345 | 0.96[ASN][1000 genomes] |
rs11788457 | 0.96[ASN][1000 genomes] |
rs11788495 | 0.96[ASN][1000 genomes] |
rs11790458 | 0.96[ASN][1000 genomes] |
rs11793356 | 0.96[ASN][1000 genomes] |
rs11793528 | 0.96[ASN][1000 genomes] |
rs11793745 | 0.96[ASN][1000 genomes] |
rs11793951 | 0.88[ASN][1000 genomes] |
rs11795175 | 0.86[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs12338315 | 0.96[ASN][1000 genomes] |
rs12350797 | 0.96[ASN][1000 genomes] |
rs12351725 | 0.96[ASN][1000 genomes] |
rs1341761 | 0.92[ASN][1000 genomes] |
rs1341762 | 0.96[ASN][1000 genomes] |
rs1361610 | 0.80[AFR][1000 genomes] |
rs16920215 | 0.96[ASN][1000 genomes] |
rs16920222 | 0.96[ASN][1000 genomes] |
rs1935236 | 0.92[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs1935237 | 0.96[ASN][1000 genomes] |
rs2226101 | 0.86[AFR][1000 genomes] |
rs2417252 | 0.96[ASN][1000 genomes] |
rs34914973 | 0.96[ASN][1000 genomes] |
rs41274981 | 0.96[ASN][1000 genomes] |
rs41274983 | 0.80[ASN][1000 genomes] |
rs41281027 | 0.96[ASN][1000 genomes] |
rs55666756 | 0.96[ASN][1000 genomes] |
rs55899105 | 0.96[ASN][1000 genomes] |
rs55995111 | 0.96[ASN][1000 genomes] |
rs56013964 | 0.96[ASN][1000 genomes] |
rs56135593 | 0.82[EUR][1000 genomes] |
rs56218982 | 0.96[ASN][1000 genomes] |
rs56251240 | 0.96[ASN][1000 genomes] |
rs56389202 | 0.96[ASN][1000 genomes] |
rs57082508 | 0.88[ASN][1000 genomes] |
rs57802761 | 0.96[ASN][1000 genomes] |
rs57833016 | 0.96[ASN][1000 genomes] |
rs58497759 | 0.96[ASN][1000 genomes] |
rs59059615 | 0.84[ASN][1000 genomes] |
rs59311341 | 0.96[ASN][1000 genomes] |
rs61040758 | 0.84[ASN][1000 genomes] |
rs7019447 | 0.96[ASN][1000 genomes] |
rs7023266 | 0.88[ASN][1000 genomes] |
rs7023837 | 0.96[ASN][1000 genomes] |
rs7023948 | 0.96[ASN][1000 genomes] |
rs7023972 | 0.96[ASN][1000 genomes] |
rs7024225 | 0.88[ASN][1000 genomes] |
rs7026000 | 0.96[ASN][1000 genomes] |
rs7034047 | 0.96[ASN][1000 genomes] |
rs7039422 | 0.96[ASN][1000 genomes] |
rs7048634 | 0.96[ASN][1000 genomes] |
rs73656609 | 0.96[ASN][1000 genomes] |
rs73656612 | 0.96[ASN][1000 genomes] |
rs73656616 | 0.96[ASN][1000 genomes] |
rs73656617 | 0.96[ASN][1000 genomes] |
rs73656618 | 0.96[ASN][1000 genomes] |
rs73656619 | 0.96[ASN][1000 genomes] |
rs73656620 | 0.96[ASN][1000 genomes] |
rs73656621 | 0.96[ASN][1000 genomes] |
rs73656622 | 0.96[ASN][1000 genomes] |
rs73656623 | 0.96[ASN][1000 genomes] |
rs73656624 | 0.96[ASN][1000 genomes] |
rs73656625 | 0.96[ASN][1000 genomes] |
rs73656626 | 0.96[ASN][1000 genomes] |
rs73656627 | 0.96[ASN][1000 genomes] |
rs73656628 | 0.96[ASN][1000 genomes] |
rs73656629 | 0.96[ASN][1000 genomes] |
rs73656630 | 0.96[ASN][1000 genomes] |
rs73656631 | 0.96[ASN][1000 genomes] |
rs73656632 | 0.96[ASN][1000 genomes] |
rs73656633 | 0.96[ASN][1000 genomes] |
rs73656635 | 0.96[ASN][1000 genomes] |
rs73656636 | 0.96[ASN][1000 genomes] |
rs73656637 | 0.96[ASN][1000 genomes] |
rs73656638 | 0.88[ASN][1000 genomes] |
rs73656639 | 0.96[ASN][1000 genomes] |
rs73656640 | 0.96[ASN][1000 genomes] |
rs73656642 | 0.96[ASN][1000 genomes] |
rs73656643 | 0.96[ASN][1000 genomes] |
rs73656644 | 0.96[ASN][1000 genomes] |
rs73656645 | 0.96[ASN][1000 genomes] |
rs73656646 | 0.96[ASN][1000 genomes] |
rs73656647 | 0.96[ASN][1000 genomes] |
rs73656648 | 0.96[ASN][1000 genomes] |
rs73656649 | 0.96[ASN][1000 genomes] |
rs73656650 | 0.96[ASN][1000 genomes] |
rs73657933 | 0.96[ASN][1000 genomes] |
rs7848855 | 0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1037157 | chr9:104045761-104149233 | Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:104098600-104104200 | Weak transcription | HepG2 | liver |