Variant report
Variant | rs13157706 |
---|---|
Chromosome Location | chr5:41041963-41041964 |
allele | A/G |
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] |
---|---|
rs1008761 | 0.82[ASN][1000 genomes] |
rs10512757 | 1.00[CHB][hapmap];0.91[ASN][1000 genomes] |
rs10512762 | 0.82[ASN][1000 genomes] |
rs10512766 | 0.88[CHB][hapmap];0.80[JPT][hapmap] |
rs11748979 | 0.82[ASN][1000 genomes] |
rs13158601 | 1.00[CHB][hapmap];0.81[JPT][hapmap] |
rs13158729 | 1.00[CHB][hapmap];0.81[JPT][hapmap];0.91[ASN][1000 genomes] |
rs13173930 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs13174484 | 0.89[CHB][hapmap] |
rs13177483 | 0.89[CHB][hapmap] |
rs13186888 | 0.91[ASN][1000 genomes] |
rs13189407 | 0.82[ASN][1000 genomes] |
rs1345800 | 1.00[CHB][hapmap];0.81[JPT][hapmap] |
rs1423390 | 0.91[ASN][1000 genomes] |
rs17198998 | 0.88[ASN][1000 genomes] |
rs17257858 | 1.00[CHB][hapmap];0.81[JPT][hapmap] |
rs17258193 | 0.91[ASN][1000 genomes] |
rs17259287 | 0.82[ASN][1000 genomes] |
rs17260165 | 1.00[CHB][hapmap];0.81[JPT][hapmap] |
rs35786815 | 0.88[ASN][1000 genomes] |
rs35807549 | 0.84[ASN][1000 genomes] |
rs35915011 | 0.82[ASN][1000 genomes] |
rs35931290 | 0.82[ASN][1000 genomes] |
rs35949425 | 0.88[ASN][1000 genomes] |
rs4552672 | 0.89[CHB][hapmap];0.81[JPT][hapmap] |
rs62360805 | 0.91[ASN][1000 genomes] |
rs6876819 | 1.00[CHB][hapmap] |
rs6898364 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72753945 | 0.82[ASN][1000 genomes] |
rs7727839 | 0.89[CHB][hapmap];0.81[JPT][hapmap] |
rs9292802 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830268 | chr5:40897361-41138366 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |