Variant report
Variant | rs11961690 |
---|---|
Chromosome Location | chr6:150436493-150436494 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:3 , 50 per page) page:
1
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rs_ID | r2[population] |
---|---|
rs11961011 | 1.00[AMR][1000 genomes] |
rs11968730 | 1.00[AMR][1000 genomes] |
rs11968865 | 1.00[AMR][1000 genomes] |
rs11969990 | 1.00[AMR][1000 genomes] |
rs1853668 | 1.00[AMR][1000 genomes] |
rs33997518 | 1.00[AMR][1000 genomes] |
rs56658443 | 1.00[AMR][1000 genomes] |
rs6921675 | 1.00[AMR][1000 genomes] |
rs6927066 | 1.00[AMR][1000 genomes] |
rs6931379 | 1.00[AMR][1000 genomes] |
rs7357003 | 1.00[AMR][1000 genomes] |
rs7771423 | 1.00[AMR][1000 genomes] |
rs9322235 | 1.00[AMR][1000 genomes] |
rs9478646 | 1.00[AMR][1000 genomes] |
rs9478651 | 1.00[AMR][1000 genomes] |
rs9766408 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv886770 | chr6:150395424-150499889 | Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv886771 | chr6:150411442-150437749 | Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv1026690 | chr6:150419115-150485583 | Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:150422400-150436800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |