Variant report
Variant | rs72771783 |
---|---|
Chromosome Location | chr5:97951616-97951617 |
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] |
---|---|
rs11953303 | 0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12187587 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17132958 | 0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17132963 | 0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17166099 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17166146 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17166151 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17166174 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17842412 | 0.82[EUR][1000 genomes] |
rs2053679 | 0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6595958 | 0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6595959 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6596179 | 0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs67468861 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6877381 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6878913 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6886015 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6890353 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs72771755 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72771766 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72771780 | 0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72771781 | 0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7701903 | 0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7711174 | 0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7712835 | 0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7732069 | 0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882412 | chr5:97796120-97953719 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1016611 | chr5:97873846-98035559 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
3 | nsv537816 | chr5:97873846-98035559 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1029509 | chr5:97888644-98040172 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv882413 | chr5:97918829-98022320 | Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | esv1832089 | chr5:97934125-97976039 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:97946400-97967200 | Weak transcription | HSMMtube | muscle |
2 | chr5:97951400-97952400 | Strong transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |