Variant report
Variant | rs11050927 |
---|---|
Chromosome Location | chr12:30648998-30648999 |
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 | chr12:30646656..30649637-chr12:30912418..30914854,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10506068 | 0.83[ASN][1000 genomes] |
rs10743721 | 0.80[ASN][1000 genomes] |
rs1500108 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1506392 | 0.83[ASN][1000 genomes] |
rs16906436 | 0.83[ASN][1000 genomes] |
rs2133690 | 0.81[ASN][1000 genomes] |
rs4931340 | 0.83[ASN][1000 genomes] |
rs4931341 | 0.82[ASN][1000 genomes] |
rs60625006 | 0.83[ASN][1000 genomes] |
rs61641938 | 0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6487915 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7131740 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7309388 | 0.81[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7960523 | 0.83[ASN][1000 genomes] |
rs7961829 | 0.83[ASN][1000 genomes] |
rs7980283 | 0.84[ASN][1000 genomes] |
rs9971884 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3343291 | chr12:30455597-30992837 | Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 48 gene(s) | inside rSNPs | diseases |
2 | nsv1050233 | chr12:30590071-30670919 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:30648800-30653600 | Strong transcription | Liver | Liver |