Variant report
Variant | rs1497516 |
---|---|
Chromosome Location | chr3:21065354-21065355 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11128983 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs13086550 | 0.86[EUR][1000 genomes] |
rs13097458 | 0.98[ASN][1000 genomes] |
rs1391138 | 0.89[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1497510 | 0.94[AFR][1000 genomes] |
rs2886728 | 0.84[EUR][1000 genomes] |
rs4306882 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4431129 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4431130 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4465961 | 0.96[ASN][1000 genomes] |
rs4858288 | 0.92[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6550561 | 0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6550562 | 0.89[EUR][1000 genomes] |
rs7612422 | 0.93[ASN][1000 genomes] |
rs7623704 | 0.93[ASN][1000 genomes] |
rs7625772 | 0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7633632 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7644744 | 0.82[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7652147 | 0.90[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs869494 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs869495 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs973870 | 0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9811079 | 0.92[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9850499 | 0.86[ASN][1000 genomes] |
rs985536 | 0.86[ASN][1000 genomes] |
rs9865061 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9881998 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv876607 | chr3:20972475-21087219 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | n/a |
2 | nsv876608 | chr3:21008710-21203048 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv998068 | chr3:21050191-21212603 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2422219 | chr3:21064893-21220097 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:21059000-21065800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr3:21065000-21065400 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |