Variant report
Variant | rs72626988 |
---|---|
Chromosome Location | chr3:68405547-68405548 |
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] |
---|---|
rs1010749 | 0.96[EUR][1000 genomes] |
rs12106777 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1388498 | 1.00[EUR][1000 genomes] |
rs1388499 | 0.96[EUR][1000 genomes] |
rs72626935 | 1.00[EUR][1000 genomes] |
rs72626936 | 1.00[EUR][1000 genomes] |
rs72626937 | 1.00[EUR][1000 genomes] |
rs72626938 | 1.00[EUR][1000 genomes] |
rs72626939 | 1.00[EUR][1000 genomes] |
rs72626956 | 1.00[EUR][1000 genomes] |
rs72626958 | 1.00[EUR][1000 genomes] |
rs72626961 | 1.00[EUR][1000 genomes] |
rs72626975 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72626976 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs72626987 | 0.98[ASN][1000 genomes] |
rs72626989 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs72626996 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs72626997 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs72627000 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs72627001 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs72628608 | 0.81[AMR][1000 genomes] |
rs957894 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752014 | chr3:68091879-68416989 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv834721 | chr3:68365963-68526394 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv590562 | chr3:68393781-68422687 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
4 | nsv590563 | chr3:68402933-68422687 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:68403200-68407800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |