Variant report
Variant | rs73059572 |
---|---|
Chromosome Location | chr1:184289029-184289030 |
allele | A/T |
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 |
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(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000207080 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10911556 | 0.85[EUR][1000 genomes] |
rs10911557 | 0.84[EUR][1000 genomes] |
rs10911560 | 0.80[EUR][1000 genomes] |
rs12069709 | 0.80[EUR][1000 genomes] |
rs12096575 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs12128914 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12727053 | 0.81[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs12727591 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs16822848 | 0.84[ASN][1000 genomes] |
rs34782871 | 0.80[EUR][1000 genomes] |
rs4618934 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs4622032 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6424946 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73059573 | 0.92[ASN][1000 genomes] |
rs7516012 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9645302 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530079 | chr1:183797938-184639971 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv528772 | chr1:184288820-184290515 | Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |