Variant report
Variant | rs7690205 |
---|---|
Chromosome Location | chr4:86452150-86452151 |
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] |
---|---|
rs10516749 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs10516751 | 0.93[YRI][hapmap];0.87[AFR][1000 genomes] |
rs1156516 | 0.92[AFR][1000 genomes] |
rs11931565 | 0.97[YRI][hapmap];0.88[AFR][1000 genomes] |
rs11932352 | 0.93[YRI][hapmap];0.89[AFR][1000 genomes] |
rs11936036 | 0.93[YRI][hapmap];0.89[AFR][1000 genomes] |
rs11936794 | 0.89[AFR][1000 genomes] |
rs11937495 | 0.87[AFR][1000 genomes] |
rs11940831 | 0.90[AFR][1000 genomes] |
rs11942163 | 0.85[AFR][1000 genomes] |
rs11945019 | 0.93[YRI][hapmap];0.90[AFR][1000 genomes] |
rs11945092 | 0.90[AFR][1000 genomes] |
rs12510337 | 0.81[AMR][1000 genomes] |
rs1481776 | 0.96[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs1481777 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1481782 | 0.81[YRI][hapmap] |
rs1540595 | 0.97[YRI][hapmap];0.93[AFR][1000 genomes] |
rs17010302 | 0.97[YRI][hapmap];0.89[AFR][1000 genomes] |
rs17010307 | 0.93[YRI][hapmap];0.87[AFR][1000 genomes] |
rs17010314 | 0.97[YRI][hapmap];0.91[AFR][1000 genomes] |
rs17010316 | 0.97[YRI][hapmap];0.91[AFR][1000 genomes] |
rs17010318 | 0.97[YRI][hapmap];0.91[AFR][1000 genomes] |
rs17010321 | 0.90[AFR][1000 genomes] |
rs17010342 | 0.96[YRI][hapmap];0.92[AFR][1000 genomes] |
rs17010356 | 0.93[YRI][hapmap];0.90[AFR][1000 genomes] |
rs17010358 | 1.00[YRI][hapmap];0.92[AFR][1000 genomes] |
rs17010365 | 1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17010389 | 0.94[YRI][hapmap];0.90[AFR][1000 genomes] |
rs17010393 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs17010402 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs17010406 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs1905033 | 0.95[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs1982699 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs1982700 | 0.93[YRI][hapmap];0.89[AFR][1000 genomes] |
rs1982701 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs1994062 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs1994063 | 0.89[AFR][1000 genomes] |
rs1994064 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs1994070 | 0.86[YRI][hapmap] |
rs1994072 | 0.83[YRI][hapmap] |
rs1994073 | 0.97[YRI][hapmap];0.88[AFR][1000 genomes] |
rs1994074 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs2869359 | 0.98[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs3919901 | 0.97[YRI][hapmap];0.93[AFR][1000 genomes] |
rs4327478 | 0.94[YRI][hapmap];0.89[AFR][1000 genomes] |
rs4327479 | 0.90[YRI][hapmap];0.89[AFR][1000 genomes] |
rs4348085 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs4391024 | 0.96[YRI][hapmap];0.90[AFR][1000 genomes] |
rs4431218 | 0.94[YRI][hapmap] |
rs4440206 | 0.90[AFR][1000 genomes] |
rs4450923 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs4450924 | 0.94[YRI][hapmap];0.88[AFR][1000 genomes] |
rs4450925 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs4525966 | 0.93[YRI][hapmap];0.89[AFR][1000 genomes] |
rs4693706 | 0.83[YRI][hapmap] |
rs58330660 | 0.88[AFR][1000 genomes] |
rs59472265 | 0.90[AFR][1000 genomes] |
rs60617422 | 0.88[AFR][1000 genomes] |
rs61658381 | 0.93[AFR][1000 genomes] |
rs6531826 | 0.97[YRI][hapmap];0.91[AFR][1000 genomes] |
rs6531828 | 0.89[YRI][hapmap];0.82[AFR][1000 genomes] |
rs6531829 | 0.90[YRI][hapmap];0.84[AFR][1000 genomes] |
rs6814596 | 0.97[YRI][hapmap];0.93[AFR][1000 genomes] |
rs6814983 | 0.97[YRI][hapmap];0.90[AFR][1000 genomes] |
rs6819251 | 1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6819986 | 0.97[YRI][hapmap];0.91[AFR][1000 genomes] |
rs6828388 | 0.86[YRI][hapmap] |
rs6828628 | 0.93[YRI][hapmap];0.88[AFR][1000 genomes] |
rs6829120 | 0.90[YRI][hapmap];0.82[AFR][1000 genomes] |
rs6829628 | 0.90[YRI][hapmap];0.82[AFR][1000 genomes] |
rs6836668 | 0.96[YRI][hapmap];0.93[AFR][1000 genomes] |
rs72967858 | 0.88[AFR][1000 genomes] |
rs72967861 | 0.88[AFR][1000 genomes] |
rs72967867 | 0.88[AFR][1000 genomes] |
rs72967869 | 0.88[AFR][1000 genomes] |
rs72967871 | 0.88[AFR][1000 genomes] |
rs73832792 | 0.82[AFR][1000 genomes] |
rs73832798 | 0.87[AFR][1000 genomes] |
rs73832799 | 0.88[AFR][1000 genomes] |
rs7685458 | 0.83[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv519588 | chr4:85762385-86591202 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv461566 | chr4:85988032-86725502 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv594747 | chr4:85988032-86725502 | Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv470048 | chr4:85998783-86720838 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:86430200-86468600 | Weak transcription | Pancreas | Pancrea |
2 | chr4:86436400-86455600 | Weak transcription | Gastric | stomach |
3 | chr4:86444400-86452600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr4:86445400-86464600 | Weak transcription | HSMM | muscle |
5 | chr4:86447800-86452200 | Weak transcription | Primary B cells from peripheral blood | blood |
6 | chr4:86449600-86453600 | Weak transcription | Primary B cells from cord blood | blood |