Variant report
Variant | rs58969648 |
---|---|
Chromosome Location | chr11:106480989-106480990 |
allele | C/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 | chr11:106480957..106482975-chr11:106532869..106534369,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11820192 | 0.91[ASN][1000 genomes] |
rs17105864 | 0.95[ASN][1000 genomes] |
rs17105870 | 0.95[ASN][1000 genomes] |
rs1938627 | 0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1938629 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1938630 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34083913 | 0.95[ASN][1000 genomes] |
rs4340012 | 0.95[ASN][1000 genomes] |
rs4582939 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs55703757 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55904925 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61095533 | 0.95[ASN][1000 genomes] |
rs7124340 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73544102 | 0.95[ASN][1000 genomes] |
rs73546004 | 0.95[ASN][1000 genomes] |
rs73546008 | 0.95[ASN][1000 genomes] |
rs73546021 | 0.95[ASN][1000 genomes] |
rs73546024 | 0.95[ASN][1000 genomes] |
rs7483143 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1048381 | chr11:105945117-106561574 | Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
2 | nsv1038836 | chr11:106459674-106514773 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv1054602 | chr11:106460454-106514773 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
4 | nsv1052457 | chr11:106477599-106507197 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:106480000-106482400 | Weak transcription | Placenta Amnion | Placenta Amnion |