Variant report
Variant | rs13235260 |
---|---|
Chromosome Location | chr7:146970312-146970313 |
allele | C/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] |
---|---|
rs10085456 | 0.87[CHB][hapmap];0.81[JPT][hapmap] |
rs10085764 | 0.90[CHB][hapmap];0.92[JPT][hapmap] |
rs1021008 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs10225100 | 1.00[CHB][hapmap];0.92[JPT][hapmap] |
rs10234386 | 1.00[CHB][hapmap];0.92[JPT][hapmap] |
rs10238730 | 0.90[CHB][hapmap];0.91[JPT][hapmap] |
rs10242430 | 0.90[CHB][hapmap];0.92[JPT][hapmap] |
rs10248220 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10251412 | 0.89[CHB][hapmap];0.88[JPT][hapmap] |
rs10261539 | 1.00[CHB][hapmap];0.92[JPT][hapmap] |
rs10262107 | 0.89[CHB][hapmap];0.90[JPT][hapmap] |
rs10268597 | 0.90[CHB][hapmap];0.91[JPT][hapmap] |
rs10276382 | 0.89[CHB][hapmap];1.00[JPT][hapmap] |
rs10278315 | 0.91[JPT][hapmap] |
rs10279700 | 0.89[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs10808044 | 1.00[CHB][hapmap];0.91[JPT][hapmap] |
rs10952678 | 1.00[CHB][hapmap];0.92[JPT][hapmap];0.98[ASN][1000 genomes] |
rs12531764 | 1.00[CHB][hapmap];0.91[JPT][hapmap] |
rs12534978 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12538316 | 0.89[CHB][hapmap];1.00[JPT][hapmap] |
rs12703895 | 1.00[CHB][hapmap];0.92[JPT][hapmap];0.98[ASN][1000 genomes] |
rs12703900 | 0.89[CHB][hapmap];0.92[JPT][hapmap] |
rs1383011 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs1390724 | 0.81[ASN][1000 genomes] |
rs1390725 | 0.91[JPT][hapmap];0.86[ASN][1000 genomes] |
rs1404707 | 1.00[CHB][hapmap];0.91[JPT][hapmap] |
rs1479837 | 0.85[CHB][hapmap] |
rs1496549 | 0.91[JPT][hapmap] |
rs1525211 | 1.00[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes] |
rs1525215 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs1525216 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17170378 | 0.92[JPT][hapmap] |
rs17170379 | 0.90[CHB][hapmap];1.00[JPT][hapmap] |
rs1917600 | 0.81[CHB][hapmap] |
rs2132591 | 0.83[JPT][hapmap] |
rs2620439 | 1.00[CHB][hapmap];0.91[JPT][hapmap] |
rs2620440 | 0.85[CHB][hapmap] |
rs2620441 | 0.85[CHB][hapmap] |
rs2692183 | 0.82[CHB][hapmap] |
rs2692186 | 0.90[CHB][hapmap];0.92[JPT][hapmap] |
rs2692187 | 1.00[CHB][hapmap];0.92[JPT][hapmap] |
rs34748606 | 0.98[ASN][1000 genomes] |
rs4637733 | 0.91[JPT][hapmap] |
rs4725708 | 0.89[JPT][hapmap] |
rs4725709 | 1.00[JPT][hapmap] |
rs4726833 | 0.91[JPT][hapmap] |
rs4726834 | 0.91[JPT][hapmap] |
rs4726835 | 0.82[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap] |
rs66602672 | 0.82[ASN][1000 genomes] |
rs6962971 | 0.83[CHB][hapmap];0.83[JPT][hapmap] |
rs6974852 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7790788 | 1.00[JPT][hapmap] |
rs885610 | 0.91[JPT][hapmap] |
rs899612 | 0.82[CHB][hapmap] |
rs899614 | 0.82[CHB][hapmap] |
rs899616 | 0.82[CHB][hapmap] |
rs9769600 | 0.91[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv933033 | chr7:146720301-147081560 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1033898 | chr7:146721499-147081768 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv931005 | chr7:146730472-147381257 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv889396 | chr7:146854133-147035067 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | esv33975 | chr7:146968440-146991336 | Enhancers Active TSS Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |