Variant report
Variant | rs973176 |
---|---|
Chromosome Location | chr2:116008808-116008809 |
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] |
---|---|
rs10185352 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10187050 | 0.91[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs10187556 | 0.80[ASN][1000 genomes] |
rs12466330 | 0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12474896 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12475000 | 0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1543147 | 0.82[AMR][1000 genomes] |
rs1607192 | 0.83[ASN][1000 genomes] |
rs17044170 | 0.89[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs17044209 | 0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4849385 | 0.91[AMR][1000 genomes] |
rs4849386 | 0.91[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs56367866 | 0.86[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs59048337 | 0.97[ASN][1000 genomes] |
rs66950432 | 0.84[ASN][1000 genomes] |
rs67201082 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs68044608 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7558115 | 0.80[ASN][1000 genomes] |
rs7562421 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7565369 | 0.91[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs7569580 | 0.85[ASN][1000 genomes] |
rs7600222 | 0.81[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014713 | chr2:115858427-116018055 | Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv1001542 | chr2:115920847-116082585 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv834339 | chr2:115953298-116132979 | Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:116008000-116013600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |