Variant report
Variant | rs73135722 |
---|---|
Chromosome Location | chr3:82205325-82205326 |
allele | G/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] |
---|---|
rs12632087 | 1.00[AMR][1000 genomes] |
rs6778193 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6778648 | 1.00[ASN][1000 genomes] |
rs6781784 | 1.00[AMR][1000 genomes] |
rs73128312 | 1.00[ASN][1000 genomes] |
rs73128314 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128319 | 1.00[ASN][1000 genomes] |
rs73128324 | 1.00[ASN][1000 genomes] |
rs73128325 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128327 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128329 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128344 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128348 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128350 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73128352 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73130394 | 1.00[ASN][1000 genomes] |
rs73132331 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73133711 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73133730 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73133743 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73135762 | 1.00[AMR][1000 genomes] |
rs73136194 | 1.00[AMR][1000 genomes] |
rs73136200 | 1.00[AMR][1000 genomes] |
rs73138120 | 1.00[AMR][1000 genomes] |
rs73138123 | 1.00[AMR][1000 genomes] |
rs73138125 | 1.00[AMR][1000 genomes] |
rs73138134 | 1.00[AMR][1000 genomes] |
rs73138138 | 1.00[AMR][1000 genomes] |
rs73138148 | 1.00[AMR][1000 genomes] |
rs73140170 | 1.00[AMR][1000 genomes] |
rs73140171 | 1.00[AMR][1000 genomes] |
rs7635749 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7643979 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9872306 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1007167 | chr3:82050178-82301466 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv877041 | chr3:82074024-82363196 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1008429 | chr3:82089650-82510536 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv432460 | chr3:82107110-82508010 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | nsv1005262 | chr3:82165228-82258781 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1013820 | chr3:82175705-82968181 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
7 | nsv877043 | chr3:82198467-82311711 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS | lncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv590779 | chr3:82203354-82223946 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:82205000-82209600 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |