Variant report
Variant | rs12583113 |
---|---|
Chromosome Location | chr13:94559716-94559717 |
allele | G/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] |
---|---|
rs1411502 | 0.86[CHB][hapmap] |
rs17174714 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs1888228 | 0.96[CEU][hapmap];0.86[CHB][hapmap] |
rs2892669 | 0.80[AFR][1000 genomes] |
rs3858844 | 0.87[AFR][1000 genomes] |
rs3904289 | 0.88[CEU][hapmap];0.86[CHB][hapmap];0.80[JPT][hapmap];0.88[EUR][1000 genomes] |
rs45608931 | 0.82[AFR][1000 genomes] |
rs61962148 | 0.82[AFR][1000 genomes] |
rs61964364 | 0.81[ASN][1000 genomes] |
rs61964366 | 0.82[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs713220 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs7997761 | 0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9516291 | 0.81[AFR][1000 genomes] |
rs9516299 | 0.82[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs9516304 | 0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[YRI][hapmap] |
rs9516307 | 0.95[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs9516309 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9524244 | 0.87[AFR][1000 genomes] |
rs9524248 | 0.87[AFR][1000 genomes] |
rs9524255 | 0.82[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs9524267 | 0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9524277 | 0.88[CEU][hapmap];0.83[YRI][hapmap];0.94[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs955129 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs9556336 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9561455 | 0.82[AFR][1000 genomes] |
rs9561456 | 0.82[AFR][1000 genomes] |
rs9561464 | 0.91[ASN][1000 genomes] |
rs9561466 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs964508 | 0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[YRI][hapmap] |
rs9796211 | 0.86[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948714 | chr13:94100104-94699435 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv933807 | chr13:94187158-94845505 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1045230 | chr13:94277683-94764671 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv948455 | chr13:94451368-94988900 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv916640 | chr13:94521959-95101443 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:94557000-94560600 | Weak transcription | Ovary | ovary |
2 | chr13:94558800-94559800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |