Variant report
Variant | rs939156 |
---|---|
Chromosome Location | chr2:190183185-190183186 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:190182192..190183759-chr2:190192942..190195754,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10190073 | 1.00[AMR][1000 genomes] |
rs10210890 | 1.00[AMR][1000 genomes] |
rs10211173 | 1.00[AMR][1000 genomes] |
rs10931399 | 1.00[AMR][1000 genomes] |
rs12693529 | 1.00[AMR][1000 genomes] |
rs1399990 | 1.00[AMR][1000 genomes] |
rs1515863 | 1.00[AMR][1000 genomes] |
rs1519180 | 1.00[AMR][1000 genomes] |
rs1818585 | 0.90[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs2037170 | 1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[AMR][1000 genomes] |
rs2037171 | 1.00[LWK][hapmap];1.00[AMR][1000 genomes] |
rs34556340 | 1.00[AMR][1000 genomes] |
rs34606082 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs3914569 | 1.00[AMR][1000 genomes] |
rs57449412 | 1.00[AMR][1000 genomes] |
rs57484527 | 1.00[AMR][1000 genomes] |
rs58082189 | 1.00[AMR][1000 genomes] |
rs58148508 | 1.00[AMR][1000 genomes] |
rs58624621 | 1.00[AMR][1000 genomes] |
rs59784139 | 1.00[AMR][1000 genomes] |
rs6434329 | 1.00[AMR][1000 genomes] |
rs6434331 | 1.00[AMR][1000 genomes] |
rs6434332 | 1.00[AMR][1000 genomes] |
rs6434333 | 1.00[AMR][1000 genomes] |
rs6434336 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6706066 | 1.00[AMR][1000 genomes] |
rs7578627 | 1.00[AMR][1000 genomes] |
rs7594988 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7606163 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533029 | chr2:189812229-190554339 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | nsv875613 | chr2:189999011-190324685 | Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
3 | nsv875614 | chr2:190110841-190254758 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:190178600-190183400 | Weak transcription | Fetal Thymus | thymus |