Variant report
Variant | rs60650957 |
---|---|
Chromosome Location | chr3:59507147-59507148 |
allele | C/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] |
---|---|
rs17060878 | 0.94[ASN][1000 genomes] |
rs17060879 | 0.94[ASN][1000 genomes] |
rs17060883 | 0.85[ASN][1000 genomes] |
rs35500604 | 0.83[ASN][1000 genomes] |
rs41502947 | 0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58468498 | 0.94[ASN][1000 genomes] |
rs72877416 | 0.94[ASN][1000 genomes] |
rs72877418 | 0.94[ASN][1000 genomes] |
rs72877421 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877424 | 0.85[ASN][1000 genomes] |
rs72877427 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877429 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877430 | 0.94[ASN][1000 genomes] |
rs72877432 | 0.94[ASN][1000 genomes] |
rs72877433 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877434 | 0.94[ASN][1000 genomes] |
rs72877437 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877442 | 0.94[ASN][1000 genomes] |
rs72877443 | 0.94[ASN][1000 genomes] |
rs72877445 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877446 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877447 | 0.94[ASN][1000 genomes] |
rs72877448 | 0.94[ASN][1000 genomes] |
rs72877450 | 0.85[ASN][1000 genomes] |
rs72877453 | 0.89[ASN][1000 genomes] |
rs72877455 | 0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72877456 | 0.94[ASN][1000 genomes] |
rs72877460 | 0.94[ASN][1000 genomes] |
rs7356070 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7638203 | 0.94[ASN][1000 genomes] |
rs7646357 | 0.94[ASN][1000 genomes] |
rs9311713 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9832635 | 0.94[ASN][1000 genomes] |
rs9840238 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9848047 | 0.91[ASN][1000 genomes] |
rs9865729 | 0.94[ASN][1000 genomes] |
rs9869699 | 0.94[ASN][1000 genomes] |
rs9870039 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1011181 | chr3:58665373-59542339 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv536574 | chr3:58665373-59542339 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv534257 | chr3:58855959-59606464 | Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
4 | nsv998676 | chr3:59485915-59519363 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv876836 | chr3:59500394-59664687 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:59505200-59508000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr3:59506800-59507200 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |