Variant report
Variant | rs980226 |
---|---|
Chromosome Location | chr2:67864313-67864314 |
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] |
---|---|
rs10196304 | 0.85[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs10490723 | 0.85[ASN][1000 genomes] |
rs12105010 | 0.82[AFR][1000 genomes] |
rs12477088 | 0.90[ASN][1000 genomes] |
rs12618268 | 0.82[ASN][1000 genomes] |
rs12987509 | 0.83[ASN][1000 genomes] |
rs12989021 | 0.83[ASN][1000 genomes] |
rs12992403 | 0.87[ASN][1000 genomes] |
rs12997331 | 0.81[ASN][1000 genomes] |
rs13003698 | 0.81[ASN][1000 genomes] |
rs13005138 | 0.82[ASN][1000 genomes] |
rs13013880 | 0.83[ASN][1000 genomes] |
rs13019532 | 0.83[ASN][1000 genomes] |
rs13021903 | 0.87[ASN][1000 genomes] |
rs13023342 | 0.81[ASN][1000 genomes] |
rs13025342 | 0.81[ASN][1000 genomes] |
rs13025376 | 0.84[ASN][1000 genomes] |
rs13028371 | 0.86[ASN][1000 genomes] |
rs1430786 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs17033996 | 0.91[ASN][1000 genomes] |
rs2861683 | 0.89[ASN][1000 genomes] |
rs2861685 | 0.89[ASN][1000 genomes] |
rs2861691 | 0.87[ASN][1000 genomes] |
rs35002785 | 0.82[ASN][1000 genomes] |
rs35179846 | 0.83[ASN][1000 genomes] |
rs35820615 | 0.82[ASN][1000 genomes] |
rs4141819 | 0.86[AFR][1000 genomes] |
rs4362542 | 0.91[ASN][1000 genomes] |
rs4671187 | 0.81[CHB][hapmap] |
rs62156279 | 0.82[ASN][1000 genomes] |
rs6546315 | 0.83[ASN][1000 genomes] |
rs6546319 | 0.91[ASN][1000 genomes] |
rs6731513 | 0.84[ASN][1000 genomes] |
rs6732490 | 0.91[ASN][1000 genomes] |
rs6746168 | 0.95[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap] |
rs6756226 | 0.90[ASN][1000 genomes] |
rs6760893 | 0.92[ASN][1000 genomes] |
rs9789546 | 0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534389 | chr2:67388428-68225338 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 36 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:67864200-67864800 | Enhancers | Psoas Muscle | Psoas |
2 | chr2:67864200-67865400 | Enhancers | Skeletal Muscle Female | skeletal muscle |
3 | chr2:67864200-67867200 | Enhancers | Skeletal Muscle Male | skeletal muscle |