Variant report
Variant | rs12225865 |
---|---|
Chromosome Location | chr11:26062852-26062853 |
allele | A/G |
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 | chr11:26060352..26062895-chr11:26083978..26086894,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10734366 | 1.00[CHB][hapmap] |
rs10742127 | 1.00[CHB][hapmap] |
rs10742128 | 1.00[CHB][hapmap] |
rs10834897 | 1.00[CHB][hapmap] |
rs10834898 | 1.00[CHB][hapmap] |
rs11029102 | 0.82[ASN][1000 genomes] |
rs11029103 | 0.91[ASN][1000 genomes] |
rs11029104 | 0.91[ASN][1000 genomes] |
rs11029106 | 0.91[ASN][1000 genomes] |
rs11029114 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11029115 | 1.00[ASN][1000 genomes] |
rs1387503 | 1.00[CHB][hapmap] |
rs1387507 | 1.00[CHB][hapmap] |
rs6484193 | 1.00[CHB][hapmap] |
rs7101817 | 1.00[CHB][hapmap] |
rs7105188 | 1.00[CHB][hapmap] |
rs7105339 | 1.00[CHB][hapmap] |
rs7115939 | 1.00[CHB][hapmap] |
rs7116083 | 1.00[CHB][hapmap] |
rs7119696 | 1.00[CHB][hapmap] |
rs7123678 | 1.00[CHB][hapmap] |
rs988513 | 1.00[CHB][hapmap] |
rs988514 | 1.00[CHB][hapmap] |
rs988516 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2760599 | chr11:25186984-26159450 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv1046507 | chr11:25469712-26111707 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1041778 | chr11:25898574-26098141 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:26060800-26065400 | Weak transcription | GM12878-XiMat | blood |