Variant report
Variant | rs16835741 |
---|---|
Chromosome Location | chr1:193715997-193715998 |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:193715834..193718393-chr1:193725574..193727798,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000237213 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs16835615 | 1.00[AMR][1000 genomes] |
rs16835664 | 1.00[AMR][1000 genomes] |
rs16835669 | 1.00[AMR][1000 genomes] |
rs16835672 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16835674 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16835693 | 1.00[AMR][1000 genomes] |
rs16835723 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16835738 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1008266 | chr1:193550185-194481053 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | esv3372415 | chr1:193612172-193988265 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv872832 | chr1:193661626-193850407 | Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv872833 | chr1:193681625-193774083 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |