Variant report
Variant | rs1409458 |
---|---|
Chromosome Location | chr13:89415966-89415967 |
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 |
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rs_ID | r2[population] |
---|---|
rs1326435 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1326440 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1326441 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1336938 | 1.00[ASN][1000 genomes] |
rs1336940 | 1.00[ASN][1000 genomes] |
rs1359656 | 1.00[ASN][1000 genomes] |
rs1409459 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs1415172 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17546413 | 1.00[ASN][1000 genomes] |
rs17628718 | 1.00[ASN][1000 genomes] |
rs1889998 | 1.00[ASN][1000 genomes] |
rs1952188 | 1.00[ASN][1000 genomes] |
rs2808807 | 0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2808808 | 0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4144008 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72638594 | 1.00[ASN][1000 genomes] |
rs72640007 | 1.00[ASN][1000 genomes] |
rs72640009 | 1.00[ASN][1000 genomes] |
rs72640048 | 1.00[ASN][1000 genomes] |
rs72640095 | 1.00[ASN][1000 genomes] |
rs72640098 | 1.00[ASN][1000 genomes] |
rs72641203 | 1.00[ASN][1000 genomes] |
rs72641204 | 1.00[ASN][1000 genomes] |
rs72641205 | 1.00[ASN][1000 genomes] |
rs72641211 | 1.00[ASN][1000 genomes] |
rs7323097 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7326906 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9301495 | 0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1043206 | chr13:89296779-89417347 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
2 | nsv900820 | chr13:89302824-89686507 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv900821 | chr13:89302824-89941209 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv1037296 | chr13:89355045-89461651 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1112 | chr13:89364975-89417543 | Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv900822 | chr13:89397027-89488821 | Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | esv3429946 | chr13:89408000-89434631 | Enhancers Bivalent Enhancer Flanking Active TSS | n/a | n/a | inside rSNPs | n/a |
8 | nsv915862 | chr13:89408920-90118030 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
9 | esv2758339 | chr13:89411081-89875974 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
10 | esv2759957 | chr13:89411081-89875974 | ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:89415800-89416600 | Enhancers | HUES64 Cell Line | embryonic stem cell |
2 | chr13:89415800-89416600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr13:89415800-89417200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |