Variant report
Variant | rs11014507 |
---|---|
Chromosome Location | chr10:25631359-25631360 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10450325 | 1.00[CHB][hapmap];1.00[CHD][hapmap] |
rs10508690 | 1.00[CHD][hapmap] |
rs10508693 | 1.00[CHB][hapmap];0.86[GIH][hapmap];0.81[TSI][hapmap] |
rs11816375 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12265226 | 1.00[CHB][hapmap];1.00[GIH][hapmap];0.82[TSI][hapmap] |
rs12359429 | 0.82[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs1329249 | 1.00[CHD][hapmap] |
rs17628278 | 1.00[CHB][hapmap] |
rs1928364 | 1.00[CHD][hapmap] |
rs1954261 | 1.00[CHD][hapmap] |
rs2026055 | 1.00[CHB][hapmap];0.92[GIH][hapmap] |
rs2480346 | 1.00[CHD][hapmap] |
rs2480350 | 1.00[CHD][hapmap] |
rs2987837 | 1.00[CHD][hapmap] |
rs3005188 | 1.00[CHD][hapmap] |
rs3005190 | 1.00[CHD][hapmap] |
rs34966230 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs35832360 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs67989843 | 0.84[EUR][1000 genomes] |
rs7904866 | 1.00[CHD][hapmap] |
rs824606 | 1.00[CHD][hapmap] |
rs866869 | 1.00[CHD][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2761583 | chr10:25525657-25722444 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | esv3349863 | chr10:25614571-25946379 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:25631200-25632400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |