Variant report
Variant | rs547545067 |
---|---|
Chromosome Location | chr12:58376724-58376725 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:4)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:4 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CTCF | chr12:58376489-58377433 | A549 | lung: | n/a | chr12:58377095-58377113 chr12:58377097-58377118 chr12:58377098-58377111 |
2 | CTCF | chr12:58376660-58376810 | NHDF-neo | bronchial: | n/a | n/a |
3 | RAD21 | chr12:58376679-58377512 | SK-N-SH | brain: | n/a | chr12:58377101-58377113 chr12:58377096-58377115 |
4 | CTCF | chr12:58376683-58377275 | HCT-116 | colon: | n/a | chr12:58377095-58377113 chr12:58377097-58377118 chr12:58377098-58377111 |
No data |
(count:2 , 50 per page) page:
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No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
RN7SKP65 | TF binding region |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv559046 | chr12:58162085-58478598 | Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 261 gene(s) | inside rSNPs | diseases |
2 | nsv523853 | chr12:58350631-58386722 | ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1051716 | chr12:58374313-58410810 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv973077 | chr12:58376473-58378422 | Enhancers Weak transcription Bivalent Enhancer | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |