Variant report
Variant | rs1511072 |
---|---|
Chromosome Location | chr6:165269709-165269710 |
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] |
---|---|
rs1511069 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1511070 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1511071 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2063427 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2063428 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs34309175 | 0.82[ASN][1000 genomes] |
rs4506023 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4569942 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4639310 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6455968 | 0.86[ASN][1000 genomes] |
rs6902206 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7356835 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7356875 | 0.80[EUR][1000 genomes] |
rs7768607 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9347936 | 0.81[ASN][1000 genomes] |
rs9365797 | 0.81[ASN][1000 genomes] |
rs9459215 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv605232 | chr6:164994771-165401154 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv830862 | chr6:165132822-165311086 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv11557 | chr6:165269422-165273754 | Enhancers Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:165269200-165270000 | Enhancers | Ovary | ovary |