Variant report
Variant | rs1107568 |
---|---|
Chromosome Location | chr8:36169108-36169109 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
RNU6-533P | TF binding region |
rs_ID | r2[population] |
---|---|
rs1107566 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1107567 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16884764 | 0.81[AFR][1000 genomes] |
rs16884807 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16884876 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16884883 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16884894 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16884902 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs41408344 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6468359 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6983120 | 0.84[AFR][1000 genomes] |
rs6984135 | 0.82[AFR][1000 genomes] |
rs6987238 | 0.82[AFR][1000 genomes] |
rs7015213 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73578572 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73586355 | 0.82[AFR][1000 genomes] |
rs73586362 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73586363 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73586366 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs73586369 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592006 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592008 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592010 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592012 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592014 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592019 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592021 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592024 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73592026 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7819939 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7831591 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7834732 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7835665 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7837634 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs879317 | 0.83[AFR][1000 genomes] |
rs879318 | 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 | nsv533420 | chr8:35358115-36227536 | Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1024552 | chr8:35655964-36210907 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv539548 | chr8:35655964-36210907 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
4 | nsv890718 | chr8:35948467-36224134 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:36167400-36170400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr8:36168600-36169400 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |