Variant report
Variant | rs13057733 |
---|---|
Chromosome Location | chr22:30455816-30455817 |
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] |
---|---|
rs1122239 | 0.89[ASN][1000 genomes] |
rs12233358 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs12484547 | 0.82[ASN][1000 genomes] |
rs13053765 | 0.85[ASN][1000 genomes] |
rs13054837 | 0.82[ASN][1000 genomes] |
rs13056332 | 0.82[ASN][1000 genomes] |
rs13057204 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs13057580 | 0.82[ASN][1000 genomes] |
rs13057878 | 0.82[ASN][1000 genomes] |
rs1476514 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs2010916 | 0.85[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs2012308 | 0.97[ASN][1000 genomes] |
rs2214047 | 0.82[ASN][1000 genomes] |
rs2412977 | 0.82[ASN][1000 genomes] |
rs2412979 | 0.82[ASN][1000 genomes] |
rs34474867 | 0.82[ASN][1000 genomes] |
rs34545612 | 0.82[ASN][1000 genomes] |
rs35710453 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs36018230 | 0.94[ASN][1000 genomes] |
rs4820829 | 0.82[ASN][1000 genomes] |
rs4823067 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs4823071 | 0.85[ASN][1000 genomes] |
rs5753002 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs5753007 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs5753013 | 0.82[ASN][1000 genomes] |
rs5753014 | 0.82[ASN][1000 genomes] |
rs5753015 | 0.82[ASN][1000 genomes] |
rs5753019 | 0.82[ASN][1000 genomes] |
rs5753020 | 0.82[ASN][1000 genomes] |
rs5753022 | 0.82[ASN][1000 genomes] |
rs5753028 | 0.82[ASN][1000 genomes] |
rs5753029 | 0.82[ASN][1000 genomes] |
rs5753030 | 0.82[ASN][1000 genomes] |
rs5763734 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs5763742 | 0.83[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs5763746 | 0.97[ASN][1000 genomes] |
rs5763748 | 0.97[ASN][1000 genomes] |
rs5763749 | 0.97[ASN][1000 genomes] |
rs5763750 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs5763758 | 0.85[ASN][1000 genomes] |
rs5763759 | 0.81[AMR][1000 genomes] |
rs5763763 | 0.85[ASN][1000 genomes] |
rs5763766 | 0.85[ASN][1000 genomes] |
rs5763769 | 0.85[ASN][1000 genomes] |
rs5763774 | 0.85[ASN][1000 genomes] |
rs5763782 | 0.85[ASN][1000 genomes] |
rs5763788 | 0.82[ASN][1000 genomes] |
rs5763805 | 0.82[ASN][1000 genomes] |
rs5763810 | 0.82[ASN][1000 genomes] |
rs5763852 | 0.82[ASN][1000 genomes] |
rs5763854 | 0.82[ASN][1000 genomes] |
rs5763861 | 0.82[ASN][1000 genomes] |
rs718773 | 0.85[ASN][1000 genomes] |
rs7286304 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs7286681 | 0.85[ASN][1000 genomes] |
rs739616 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs757026 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs766011 | 0.82[ASN][1000 genomes] |
rs975704 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1064081 | chr22:29826745-30623965 | Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
2 | nsv544677 | chr22:29826745-30623965 | Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
3 | nsv829165 | chr22:30450894-30459421 | Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv819812 | chr22:30453933-30470372 | Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr22:30452600-30456200 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |