Variant report
Variant | rs11845184 |
---|---|
Chromosome Location | chr14:81487858-81487859 |
allele | A/G |
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:
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No data |
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rs_ID | r2[population] |
---|---|
rs10130150 | 1.00[MEX][hapmap] |
rs10133525 | 0.90[AMR][1000 genomes] |
rs10136949 | 0.90[AMR][1000 genomes] |
rs10137669 | 1.00[MEX][hapmap] |
rs10138961 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10139168 | 0.90[AMR][1000 genomes] |
rs10141257 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10149425 | 1.00[MEX][hapmap];0.90[AMR][1000 genomes] |
rs10150439 | 0.88[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs10152059 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11844944 | 0.80[AMR][1000 genomes] |
rs11847561 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11847808 | 0.90[AMR][1000 genomes] |
rs11850795 | 0.90[AMR][1000 genomes] |
rs11850804 | 0.90[AMR][1000 genomes] |
rs11850866 | 0.90[AMR][1000 genomes] |
rs11850934 | 0.90[AMR][1000 genomes] |
rs11851697 | 1.00[MEX][hapmap] |
rs12587252 | 1.00[MEX][hapmap] |
rs28376437 | 0.90[AMR][1000 genomes] |
rs28504619 | 0.90[AMR][1000 genomes] |
rs28533809 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28534062 | 0.90[AMR][1000 genomes] |
rs28685026 | 0.90[AMR][1000 genomes] |
rs28701160 | 0.90[AMR][1000 genomes] |
rs59265535 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes] |
rs60983251 | 0.90[AMR][1000 genomes] |
rs7144235 | 0.80[AMR][1000 genomes] |
rs7144496 | 0.90[AMR][1000 genomes] |
rs7147361 | 0.90[AMR][1000 genomes] |
rs7147838 | 0.90[AMR][1000 genomes] |
rs7147839 | 0.90[AMR][1000 genomes] |
rs7148019 | 0.90[AMR][1000 genomes] |
rs7152740 | 1.00[MEX][hapmap] |
rs7160338 | 0.90[AMR][1000 genomes] |
rs74064761 | 0.90[AMR][1000 genomes] |
rs74064762 | 0.90[AMR][1000 genomes] |
rs74064776 | 0.90[AMR][1000 genomes] |
rs74064781 | 0.90[AMR][1000 genomes] |
rs74064786 | 0.90[AMR][1000 genomes] |
rs74064794 | 0.90[AMR][1000 genomes] |
rs8010771 | 0.90[AMR][1000 genomes] |
rs8010968 | 1.00[MEX][hapmap] |
rs8015542 | 1.00[MEX][hapmap] |
rs9323695 | 1.00[MEX][hapmap] |
rs9323696 | 0.90[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869348 | chr14:80921098-81535754 | Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv1052999 | chr14:81468860-81599074 | Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
3 | nsv542144 | chr14:81468860-81599074 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:81455800-81492200 | Weak transcription | Fetal Thymus | thymus |
2 | chr14:81484600-81502400 | Weak transcription | Liver | Liver |
3 | chr14:81487000-81489600 | Weak transcription | Dnd41 | blood |
4 | chr14:81487000-81498600 | Weak transcription | Thymus | Thymus |
5 | chr14:81487800-81488600 | Weak transcription | K562 | blood |