Variant report
Variant | rs13391905 |
---|---|
Chromosome Location | chr2:142247707-142247708 |
allele | A/C |
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] |
---|---|
rs10169644 | 0.80[CHB][hapmap] |
rs10173806 | 0.85[CEU][hapmap] |
rs10184273 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10204518 | 0.92[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10496882 | 0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11895715 | 0.82[CEU][hapmap] |
rs34333390 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4264514 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4327189 | 0.85[CEU][hapmap] |
rs4335888 | 0.82[CEU][hapmap] |
rs4338922 | 0.80[EUR][1000 genomes] |
rs4340449 | 0.81[CEU][hapmap];0.80[EUR][1000 genomes] |
rs4416160 | 0.85[CEU][hapmap] |
rs4430882 | 0.82[CEU][hapmap] |
rs4446018 | 0.84[CEU][hapmap] |
rs4446019 | 0.81[CEU][hapmap] |
rs4507040 | 0.81[CEU][hapmap] |
rs4531869 | 0.82[CEU][hapmap] |
rs4574058 | 0.98[ASN][1000 genomes] |
rs4583399 | 0.82[CEU][hapmap];0.81[EUR][1000 genomes] |
rs4591293 | 0.81[JPT][hapmap] |
rs4599051 | 0.81[CEU][hapmap] |
rs4954912 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4954916 | 0.81[CHB][hapmap];1.00[JPT][hapmap] |
rs5012231 | 0.82[CEU][hapmap] |
rs6429886 | 0.84[CEU][hapmap] |
rs6718919 | 0.81[CEU][hapmap] |
rs6719026 | 0.84[CEU][hapmap] |
rs6723276 | 1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap] |
rs6733981 | 0.82[CEU][hapmap] |
rs6759197 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72849648 | 1.00[ASN][1000 genomes] |
rs7585091 | 0.82[JPT][hapmap] |
rs9287318 | 1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9287319 | 0.80[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817518 | chr2:141714174-142287302 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv583203 | chr2:142055133-142378975 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv875234 | chr2:142156180-142254119 | Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
4 | nsv875240 | chr2:142199421-142347455 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
5 | nsv875243 | chr2:142219033-142259592 | Enhancers Weak transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
6 | nsv459607 | chr2:142226768-142263400 | Enhancers Weak transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
7 | nsv583207 | chr2:142226768-142263400 | Enhancers Weak transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
8 | nsv459618 | chr2:142246988-142263746 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
9 | nsv583209 | chr2:142246988-142263746 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:142239400-142256400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr2:142247400-142249600 | Enhancers | Brain Angular Gyrus | brain |
3 | chr2:142247400-142249600 | Enhancers | Brain Substantia Nigra | brain |
4 | chr2:142247600-142247800 | Enhancers | Brain Anterior Caudate | brain |