Variant report
Variant | rs61942833 |
---|---|
Chromosome Location | chr12:48844674-48844675 |
allele | A/C |
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] |
---|---|
rs11168572 | 0.85[ASN][1000 genomes] |
rs11168584 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs11168601 | 0.83[AFR][1000 genomes] |
rs11611327 | 0.82[EUR][1000 genomes] |
rs11612896 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs11829869 | 0.81[AFR][1000 genomes] |
rs11830262 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs11832311 | 0.81[AFR][1000 genomes] |
rs11833650 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs11834979 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs11836257 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs11837374 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs12318285 | 0.93[EUR][1000 genomes] |
rs12424940 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs17123105 | 0.83[AFR][1000 genomes] |
rs17123106 | 0.83[AFR][1000 genomes] |
rs17123108 | 0.83[AFR][1000 genomes] |
rs2068293 | 0.83[AFR][1000 genomes] |
rs34400124 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs4146339 | 0.84[ASN][1000 genomes] |
rs4146340 | 0.84[ASN][1000 genomes] |
rs4265629 | 0.83[AFR][1000 genomes] |
rs4500527 | 0.81[AFR][1000 genomes] |
rs56053566 | 0.91[EUR][1000 genomes] |
rs56413025 | 0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56796388 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs72644858 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs72644859 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs72644862 | 0.81[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs72644863 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs72644864 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs72644865 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv427911 | chr12:48670336-48979396 | Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | diseases |
2 | nsv832402 | chr12:48686761-48851020 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
3 | nsv977157 | chr12:48839854-48852791 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:48844600-48845000 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |