Variant report
Variant | rs1748801 |
---|---|
Chromosome Location | chr6:49221992-49221993 |
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] |
---|---|
rs16878821 | 1.00[EUR][1000 genomes] |
rs1924993 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59675093 | 1.00[EUR][1000 genomes] |
rs59931512 | 1.00[EUR][1000 genomes] |
rs61271016 | 1.00[EUR][1000 genomes] |
rs6902534 | 1.00[EUR][1000 genomes] |
rs6924438 | 1.00[EUR][1000 genomes] |
rs6931146 | 1.00[EUR][1000 genomes] |
rs73431717 | 1.00[EUR][1000 genomes] |
rs73431726 | 1.00[EUR][1000 genomes] |
rs73431759 | 1.00[EUR][1000 genomes] |
rs73431775 | 1.00[EUR][1000 genomes] |
rs73474745 | 1.00[EUR][1000 genomes] |
rs73474755 | 1.00[EUR][1000 genomes] |
rs73474763 | 1.00[EUR][1000 genomes] |
rs73485275 | 1.00[EUR][1000 genomes] |
rs73485281 | 1.00[EUR][1000 genomes] |
rs73485283 | 1.00[EUR][1000 genomes] |
rs73485296 | 1.00[EUR][1000 genomes] |
rs7751901 | 1.00[EUR][1000 genomes] |
rs7774729 | 1.00[EUR][1000 genomes] |
rs9918455 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949690 | chr6:48595821-49289855 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | esv2755862 | chr6:49081541-49298041 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:49221400-49223400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |