Variant report
Variant | rs443368 |
---|---|
Chromosome Location | chr13:62864179-62864180 |
allele | A/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] |
---|---|
rs1752812 | 0.82[ASN][1000 genomes] |
rs2034288 | 0.87[EUR][1000 genomes] |
rs3118814 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs3118816 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs3118817 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs3118824 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3118825 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs3128055 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs423113 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs5020678 | 0.84[EUR][1000 genomes] |
rs5020679 | 0.84[EUR][1000 genomes] |
rs5020680 | 0.84[EUR][1000 genomes] |
rs5020681 | 0.85[EUR][1000 genomes] |
rs66824322 | 0.86[EUR][1000 genomes] |
rs7139822 | 0.96[CEU][hapmap];0.87[CHB][hapmap] |
rs7320109 | 0.84[EUR][1000 genomes] |
rs7320115 | 0.84[EUR][1000 genomes] |
rs7323089 | 0.96[CEU][hapmap];0.87[CHB][hapmap] |
rs7981757 | 0.87[EUR][1000 genomes] |
rs7982438 | 0.87[EUR][1000 genomes] |
rs7982706 | 0.87[EUR][1000 genomes] |
rs7983039 | 0.87[EUR][1000 genomes] |
rs7983391 | 0.87[EUR][1000 genomes] |
rs7987611 | 0.87[EUR][1000 genomes] |
rs7988008 | 0.87[EUR][1000 genomes] |
rs7989138 | 0.87[EUR][1000 genomes] |
rs7994456 | 0.86[EUR][1000 genomes] |
rs7995805 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs8001256 | 0.87[EUR][1000 genomes] |
rs9285236 | 0.87[EUR][1000 genomes] |
rs9317229 | 0.85[EUR][1000 genomes] |
rs950159 | 0.96[CEU][hapmap];0.87[CHB][hapmap] |
rs9528477 | 0.84[EUR][1000 genomes] |
rs9528478 | 0.83[EUR][1000 genomes] |
rs9528494 | 0.87[EUR][1000 genomes] |
rs9528495 | 0.87[EUR][1000 genomes] |
rs9528496 | 0.87[EUR][1000 genomes] |
rs9528497 | 0.86[EUR][1000 genomes] |
rs9528498 | 0.86[EUR][1000 genomes] |
rs9528499 | 0.86[EUR][1000 genomes] |
rs9528503 | 0.96[CEU][hapmap];0.86[CHB][hapmap] |
rs9539442 | 0.84[EUR][1000 genomes] |
rs9539443 | 0.84[EUR][1000 genomes] |
rs9539452 | 0.87[EUR][1000 genomes] |
rs9539453 | 0.87[EUR][1000 genomes] |
rs9539454 | 0.87[EUR][1000 genomes] |
rs9539455 | 0.87[EUR][1000 genomes] |
rs9539456 | 0.87[EUR][1000 genomes] |
rs9539462 | 0.96[CEU][hapmap];0.87[CHB][hapmap] |
rs9539467 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948810 | chr13:62003256-62968196 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv900257 | chr13:62782367-62907090 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv561893 | chr13:62807570-62885877 | Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats | lncRNA | n/a | inside rSNPs | diseases |
4 | nsv1038992 | chr13:62827929-63369497 | Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
5 | nsv541795 | chr13:62827929-63369497 | Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
6 | nsv1038215 | chr13:62836702-63405446 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:62863400-62864600 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr13:62863600-62864600 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |