Variant report
Variant | rs17075154 |
---|---|
Chromosome Location | chr6:113760888-113760889 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000232316 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10484456 | 1.00[EUR][1000 genomes] |
rs10484460 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17075210 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2068614 | 1.00[EUR][1000 genomes] |
rs2068615 | 1.00[EUR][1000 genomes] |
rs55715533 | 1.00[EUR][1000 genomes] |
rs55812012 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56098259 | 1.00[EUR][1000 genomes] |
rs57194334 | 1.00[AMR][1000 genomes] |
rs57950622 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60729491 | 1.00[AMR][1000 genomes] |
rs73539771 | 1.00[EUR][1000 genomes] |
rs73765209 | 1.00[EUR][1000 genomes] |
rs73765210 | 1.00[EUR][1000 genomes] |
rs73765212 | 1.00[EUR][1000 genomes] |
rs73765216 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73765218 | 1.00[AMR][1000 genomes] |
rs7740950 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9488173 | 1.00[EUR][1000 genomes] |
rs9488201 | 1.00[EUR][1000 genomes] |
rs9918448 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916294 | chr6:113518489-113904305 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv1034256 | chr6:113703567-113793790 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1021815 | chr6:113703567-113799956 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1018357 | chr6:113748468-113781070 | Weak transcription Flanking Active TSS Enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv518991 | chr6:113760526-113799618 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:113755800-113767800 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
2 | chr6:113756200-113762800 | Weak transcription | A549 | lung |