Variant report
Variant | rs12695321 |
---|---|
Chromosome Location | chr3:115848515-115848516 |
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] |
---|---|
rs10212350 | 0.93[YRI][hapmap];0.81[AFR][1000 genomes] |
rs11425708 | 0.83[AMR][1000 genomes] |
rs13318106 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1344131 | 0.93[CEU][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs17697994 | 0.93[CEU][hapmap];0.94[EUR][1000 genomes] |
rs1920379 | 0.87[CEU][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs2222827 | 0.87[CEU][hapmap];0.94[EUR][1000 genomes] |
rs34930794 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35914238 | 0.94[EUR][1000 genomes] |
rs4263291 | 0.92[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs4831229 | 0.93[CEU][hapmap];0.95[EUR][1000 genomes] |
rs4831230 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs5004406 | 0.88[CEU][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs56121547 | 0.94[EUR][1000 genomes] |
rs62269168 | 0.86[EUR][1000 genomes] |
rs62269170 | 0.94[EUR][1000 genomes] |
rs6438298 | 0.90[YRI][hapmap] |
rs66490447 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73139202 | 0.93[EUR][1000 genomes] |
rs7632265 | 0.93[CEU][hapmap];0.95[EUR][1000 genomes] |
rs9283565 | 0.96[YRI][hapmap];0.80[AFR][1000 genomes] |
rs9289044 | 0.80[AFR][1000 genomes] |
rs9809229 | 1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9813038 | 0.83[EUR][1000 genomes] |
rs9821865 | 0.83[AMR][1000 genomes] |
rs9827733 | 0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9837276 | 0.84[CEU][hapmap] |
rs9857520 | 0.87[CEU][hapmap];0.93[EUR][1000 genomes] |
rs9866484 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs9866658 | 0.93[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9868784 | 0.88[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9873576 | 0.81[CEU][hapmap] |
rs9877662 | 0.93[EUR][1000 genomes] |
rs9985471 | 0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1012260 | chr3:115680931-115935968 | Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | esv2756413 | chr3:115721898-115908480 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
3 | esv2751975 | chr3:115766285-115902901 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
4 | esv2755046 | chr3:115818840-115942952 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
5 | nsv591345 | chr3:115819376-115902901 | Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | esv2752728 | chr3:115833212-115902901 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:115846000-115851200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
2 | chr3:115847400-115849400 | Enhancers | Pancreatic Islets | Pancreatic Islet |
3 | chr3:115848000-115848600 | Enhancers | Liver | Liver |
4 | chr3:115848400-115848800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |