Variant report
Variant | rs73205898 |
---|---|
Chromosome Location | chr13:61698316-61698317 |
allele | A/G |
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] |
---|---|
rs10507661 | 0.87[EUR][1000 genomes] |
rs10507662 | 0.89[EUR][1000 genomes] |
rs17059292 | 0.87[EUR][1000 genomes] |
rs17059306 | 0.87[EUR][1000 genomes] |
rs17059308 | 0.87[EUR][1000 genomes] |
rs17059315 | 0.83[EUR][1000 genomes] |
rs17059374 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4509905 | 0.83[EUR][1000 genomes] |
rs68086859 | 0.80[EUR][1000 genomes] |
rs73205840 | 0.83[EUR][1000 genomes] |
rs73205847 | 0.87[EUR][1000 genomes] |
rs73205850 | 0.89[EUR][1000 genomes] |
rs73205852 | 0.89[EUR][1000 genomes] |
rs73205854 | 0.89[EUR][1000 genomes] |
rs73205855 | 0.89[EUR][1000 genomes] |
rs73205856 | 0.89[EUR][1000 genomes] |
rs73205861 | 0.89[EUR][1000 genomes] |
rs73205865 | 0.89[EUR][1000 genomes] |
rs73205866 | 0.89[EUR][1000 genomes] |
rs73205870 | 0.89[EUR][1000 genomes] |
rs73205873 | 0.89[EUR][1000 genomes] |
rs73205877 | 0.89[EUR][1000 genomes] |
rs73205880 | 0.89[EUR][1000 genomes] |
rs73205890 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs73205891 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs73205892 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs73205893 | 1.00[ASN][1000 genomes] |
rs73208210 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs73208223 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs73208228 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73208231 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73208233 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73208235 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73208238 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs73208241 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs73208251 | 0.82[EUR][1000 genomes] |
rs9317156 | 0.89[EUR][1000 genomes] |
rs9563858 | 0.83[EUR][1000 genomes] |
rs9563859 | 0.87[EUR][1000 genomes] |
rs9563860 | 0.87[EUR][1000 genomes] |
rs9563861 | 0.87[EUR][1000 genomes] |
rs9563862 | 0.83[EUR][1000 genomes] |
rs9563863 | 0.87[EUR][1000 genomes] |
rs9563864 | 0.89[EUR][1000 genomes] |
rs9563865 | 0.89[EUR][1000 genomes] |
rs9563866 | 0.89[EUR][1000 genomes] |
rs9563867 | 0.89[EUR][1000 genomes] |
rs9570420 | 0.82[EUR][1000 genomes] |
rs9570423 | 0.82[EUR][1000 genomes] |
rs9570425 | 0.87[EUR][1000 genomes] |
rs9570426 | 0.87[EUR][1000 genomes] |
rs9570427 | 0.87[EUR][1000 genomes] |
rs9570429 | 0.87[EUR][1000 genomes] |
rs9570431 | 0.87[EUR][1000 genomes] |
rs9570432 | 0.87[EUR][1000 genomes] |
rs9570433 | 0.83[EUR][1000 genomes] |
rs9570434 | 0.87[EUR][1000 genomes] |
rs9570438 | 0.87[EUR][1000 genomes] |
rs9570440 | 0.89[EUR][1000 genomes] |
rs9570444 | 0.89[EUR][1000 genomes] |
rs9570446 | 0.89[EUR][1000 genomes] |
rs9570451 | 0.85[EUR][1000 genomes] |
rs9570457 | 0.93[EUR][1000 genomes] |
rs9570460 | 1.00[AFR][1000 genomes];0.93[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832627 | chr13:61642811-61829217 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 1 gene(s) | inside rSNPs | diseases |
2 | esv3444432 | chr13:61665252-61781081 | Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:61694400-61699800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr13:61698000-61698400 | Enhancers | H1 Cell Line | embryonic stem cell |
3 | chr13:61698000-61698400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
4 | chr13:61698000-61698600 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
5 | chr13:61698200-61698400 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |