Variant report
Variant | rs1039692 |
---|---|
Chromosome Location | chr6:54630866-54630867 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:54627133..54632625-chr6:54707387..54713886,8 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
KRASP1 | TF binding region |
ENSG00000168143 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1039696 | 1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs17448241 | 1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs17545325 | 1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs2063116 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes] |
rs2063117 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes] |
rs55776188 | 0.96[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs56054254 | 0.96[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73742805 | 0.96[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73743759 | 0.96[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7762869 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes] |
rs949796 | 1.00[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv885900 | chr6:54517968-54852462 | Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv885901 | chr6:54588069-54635417 | Enhancers Weak transcription Strong transcription Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv885902 | chr6:54588069-54656673 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |