Variant report
Variant | rs10188231 |
---|---|
Chromosome Location | chr2:142297493-142297494 |
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] |
---|---|
rs10182090 | 0.81[CHB][hapmap];0.88[JPT][hapmap] |
rs10188429 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10496885 | 1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10496887 | 0.87[CEU][hapmap] |
rs10928103 | 0.93[JPT][hapmap] |
rs10928104 | 0.93[JPT][hapmap] |
rs11677045 | 1.00[JPT][hapmap] |
rs12052672 | 0.93[CHB][hapmap];0.88[JPT][hapmap];0.82[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs12464897 | 1.00[JPT][hapmap] |
rs12472911 | 1.00[JPT][hapmap] |
rs12618990 | 1.00[JPT][hapmap] |
rs13008033 | 1.00[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13394458 | 0.94[JPT][hapmap] |
rs13397685 | 1.00[CEU][hapmap];0.85[JPT][hapmap] |
rs13401279 | 1.00[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.84[YRI][hapmap] |
rs13408702 | 0.93[JPT][hapmap] |
rs13415966 | 0.93[JPT][hapmap] |
rs13419567 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13431681 | 0.87[CEU][hapmap] |
rs1384660 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap] |
rs1471673 | 0.88[CEU][hapmap] |
rs1483149 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs1483153 | 0.88[CEU][hapmap] |
rs17551974 | 1.00[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3935991 | 1.00[JPT][hapmap] |
rs3936044 | 1.00[JPT][hapmap] |
rs3936045 | 1.00[JPT][hapmap] |
rs4073067 | 0.93[JPT][hapmap] |
rs4287717 | 0.88[CEU][hapmap] |
rs4401160 | 0.86[JPT][hapmap] |
rs6429884 | 1.00[JPT][hapmap] |
rs6429914 | 0.87[CEU][hapmap] |
rs6733988 | 0.88[JPT][hapmap] |
rs6739919 | 0.94[CEU][hapmap] |
rs6752894 | 0.94[CEU][hapmap] |
rs67536595 | 0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7575223 | 0.87[CEU][hapmap] |
rs7584391 | 1.00[CEU][hapmap];0.93[CHB][hapmap];0.88[JPT][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs879272 | 0.88[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | 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 |
2 | 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 |
3 | nsv470491 | chr2:142254119-142299923 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
4 | nsv834393 | chr2:142256714-142431564 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | n/a |
5 | nsv583212 | chr2:142263979-142309330 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
6 | nsv459640 | chr2:142291211-142345574 | Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
7 | nsv583213 | chr2:142291211-142345574 | Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:142296200-142298400 | Enhancers | Muscle Satellite Cultured Cells | -- |