Variant report
Variant | rs4506713 |
---|---|
Chromosome Location | chr12:41627699-41627700 |
allele | A/G |
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] |
---|---|
rs10506182 | 0.96[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs10748275 | 0.94[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs10785150 | 0.86[ASN][1000 genomes] |
rs10785174 | 0.93[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs10785177 | 0.96[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs10879889 | 0.96[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs11180421 | 0.93[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs1346905 | 0.86[ASN][1000 genomes] |
rs1367600 | 0.95[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs1405548 | 0.93[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs1431102 | 0.85[ASN][1000 genomes] |
rs1431108 | 0.86[ASN][1000 genomes] |
rs1431114 | 0.96[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs1431115 | 0.96[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs1431116 | 0.81[ASN][1000 genomes] |
rs1852461 | 0.94[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs1870704 | 0.87[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs1966609 | 0.81[ASN][1000 genomes] |
rs2060053 | 0.96[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs2060054 | 0.96[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs2060055 | 0.96[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs2195706 | 0.94[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs2897227 | 0.84[ASN][1000 genomes] |
rs2897228 | 0.94[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs3911712 | 0.86[ASN][1000 genomes] |
rs4278570 | 0.95[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs4768336 | 0.80[AFR][1000 genomes] |
rs6582280 | 0.94[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs6582281 | 0.91[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs6582282 | 0.94[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs6582283 | 0.92[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs7137842 | 0.92[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs7304286 | 0.96[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs7487688 | 0.86[ASN][1000 genomes] |
rs7961556 | 0.92[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs7961657 | 0.91[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs7980599 | 0.86[ASN][1000 genomes] |
rs9788073 | 0.95[AFR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv497867 | chr12:41286305-41728650 | Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv427910 | chr12:41374913-41650593 | Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1051524 | chr12:41409977-41643387 | Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv899034 | chr12:41515090-41698342 | Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv899035 | chr12:41548545-41710912 | Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:41623200-41635600 | Weak transcription | Colon Smooth Muscle | Colon |
2 | chr12:41623600-41637000 | Weak transcription | Ovary | ovary |