Variant report
Variant | rs11181289 |
---|---|
Chromosome Location | chr12:42402342-42402343 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr12:42397177..42399154-chr12:42402101..42403681,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1059360 | 0.86[CHB][hapmap] |
rs10785333 | 0.86[CHB][hapmap] |
rs10880220 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10880230 | 0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10880259 | 0.83[CHB][hapmap] |
rs10880260 | 0.90[CHB][hapmap] |
rs10880261 | 0.83[CHB][hapmap] |
rs10880264 | 0.81[CHB][hapmap] |
rs10880268 | 0.86[CHB][hapmap] |
rs11181308 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs11181328 | 0.87[CEU][hapmap];1.00[CHB][hapmap] |
rs11181364 | 0.81[CHB][hapmap] |
rs12371615 | 0.86[CHB][hapmap] |
rs12372597 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3229 | 0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7312933 | 0.92[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap] |
rs7957213 | 0.93[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7969415 | 0.94[AMR][1000 genomes];0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv430505 | chr12:42297931-42720773 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | nsv832387 | chr12:42345541-42465505 | Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:42402000-42402400 | Active TSS | K562 | blood |