Variant report
Variant | rs2052344 |
---|---|
Chromosome Location | chr8:113205436-113205437 |
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] |
---|---|
rs1019350 | 0.81[CEU][hapmap];0.82[JPT][hapmap] |
rs10505176 | 0.86[CEU][hapmap] |
rs10955617 | 0.87[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs10955618 | 0.86[CEU][hapmap] |
rs1158895 | 0.86[CEU][hapmap] |
rs11775013 | 0.86[CEU][hapmap] |
rs11778155 | 0.92[CEU][hapmap] |
rs11778209 | 0.86[CEU][hapmap] |
rs11778262 | 0.86[CEU][hapmap];0.81[JPT][hapmap] |
rs11778443 | 0.87[CEU][hapmap] |
rs11778532 | 0.93[CEU][hapmap];0.80[JPT][hapmap] |
rs11782384 | 0.88[CEU][hapmap] |
rs11783119 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11783495 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs11784683 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs11785270 | 0.88[CEU][hapmap] |
rs11785419 | 0.86[CEU][hapmap] |
rs11786836 | 0.85[EUR][1000 genomes] |
rs11989521 | 0.82[EUR][1000 genomes] |
rs1420857 | 0.88[CEU][hapmap] |
rs1420861 | 0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1492676 | 0.88[CEU][hapmap] |
rs16883301 | 0.94[CEU][hapmap];0.87[JPT][hapmap];0.81[EUR][1000 genomes] |
rs16883320 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs16883325 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs16883359 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs16883360 | 0.86[CEU][hapmap];0.81[JPT][hapmap] |
rs16883401 | 0.88[CEU][hapmap] |
rs16883404 | 0.88[CEU][hapmap] |
rs16883432 | 0.88[CEU][hapmap] |
rs16883437 | 0.86[CEU][hapmap] |
rs16883454 | 0.88[CEU][hapmap] |
rs16883506 | 0.86[CEU][hapmap] |
rs1861753 | 0.87[JPT][hapmap];0.81[EUR][1000 genomes] |
rs1861754 | 0.93[CEU][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes] |
rs1861755 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs1948411 | 0.88[CEU][hapmap] |
rs1994795 | 0.88[CEU][hapmap] |
rs1994796 | 0.81[CEU][hapmap] |
rs2052339 | 0.87[CEU][hapmap];0.81[JPT][hapmap] |
rs2098455 | 0.94[CEU][hapmap];0.87[JPT][hapmap];0.81[EUR][1000 genomes] |
rs2111426 | 0.86[CEU][hapmap];0.81[JPT][hapmap] |
rs2201203 | 0.86[CEU][hapmap] |
rs2353271 | 0.87[CEU][hapmap] |
rs3922407 | 0.86[CEU][hapmap];0.81[JPT][hapmap] |
rs6415459 | 0.88[CEU][hapmap];0.82[JPT][hapmap] |
rs6469409 | 0.94[EUR][1000 genomes] |
rs7820425 | 0.88[CEU][hapmap] |
rs7825635 | 0.88[CEU][hapmap] |
rs7826270 | 0.86[CEU][hapmap] |
rs7827158 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7844829 | 1.00[CEU][hapmap] |
rs888254 | 0.86[CEU][hapmap];0.81[JPT][hapmap] |
rs929686 | 0.86[CEU][hapmap] |
rs950983 | 0.81[EUR][1000 genomes] |
rs990616 | 0.86[CEU][hapmap];0.81[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533857 | chr8:112819659-113801258 | Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv891321 | chr8:112978128-113229425 | Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv891322 | chr8:112978128-113267916 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1022457 | chr8:113071774-113811177 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:113205000-113207200 | Enhancers | Skeletal Muscle Male | skeletal muscle |
2 | chr8:113205200-113207200 | Enhancers | Skeletal Muscle Female | skeletal muscle |