Variant report
Variant | rs73597730 |
---|---|
Chromosome Location | chr20:15937545-15937546 |
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] |
---|---|
rs1012299 | 0.93[ASN][1000 genomes] |
rs16996802 | 0.93[ASN][1000 genomes] |
rs16996835 | 0.93[ASN][1000 genomes] |
rs16996850 | 0.93[ASN][1000 genomes] |
rs16996861 | 0.93[ASN][1000 genomes] |
rs16996862 | 0.93[ASN][1000 genomes] |
rs16996864 | 0.93[ASN][1000 genomes] |
rs6074980 | 0.93[AFR][1000 genomes] |
rs6080052 | 0.90[AFR][1000 genomes] |
rs6105495 | 0.87[EUR][1000 genomes] |
rs6105497 | 0.87[EUR][1000 genomes] |
rs6105498 | 0.87[EUR][1000 genomes] |
rs6110837 | 0.87[EUR][1000 genomes] |
rs6110847 | 0.93[AFR][1000 genomes] |
rs73597720 | 0.93[ASN][1000 genomes] |
rs73597721 | 0.93[ASN][1000 genomes] |
rs73597722 | 0.93[ASN][1000 genomes] |
rs73597723 | 0.93[ASN][1000 genomes] |
rs73597724 | 0.93[ASN][1000 genomes] |
rs73597725 | 0.93[ASN][1000 genomes] |
rs73597726 | 0.93[ASN][1000 genomes] |
rs73597727 | 0.93[ASN][1000 genomes] |
rs73597728 | 0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs73597729 | 0.93[ASN][1000 genomes] |
rs73597731 | 0.93[ASN][1000 genomes] |
rs73597732 | 0.93[ASN][1000 genomes] |
rs73597734 | 0.93[ASN][1000 genomes] |
rs73597735 | 0.93[ASN][1000 genomes] |
rs73597737 | 0.93[ASN][1000 genomes] |
rs73597738 | 0.93[ASN][1000 genomes] |
rs73597739 | 0.93[ASN][1000 genomes] |
rs73597741 | 0.93[ASN][1000 genomes] |
rs73597743 | 0.93[ASN][1000 genomes] |
rs957159 | 0.93[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv833929 | chr20:15765372-15977337 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | esv3447866 | chr20:15799286-16115291 | Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15923000-15951200 | Weak transcription | Primary B cells from peripheral blood | blood |
2 | chr20:15924200-15938400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
3 | chr20:15937200-15940600 | Weak transcription | Primary B cells from cord blood | blood |