Variant report
Variant | rs72672271 |
---|---|
Chromosome Location | chr1:59024526-59024527 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:59010806..59014775-chr1:59020178..59025032,4 | MCF-7 | breast: | |
2 | chr1:59005153..59007258-chr1:59023962..59025940,2 | K562 | blood: | |
3 | chr1:59023125..59024763-chr1:59041527..59043694,2 | MCF-7 | breast: | |
4 | chr1:59010754..59013570-chr1:59022178..59025066,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000173406 | Chromatin interaction |
ENSG00000162600 | Chromatin interaction |
ENSG00000184292 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1062964 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs14008 | 0.80[EUR][1000 genomes] |
rs2268943 | 0.83[EUR][1000 genomes] |
rs55731318 | 1.00[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs56065191 | 0.86[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs56381640 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs58370530 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6671358 | 0.83[AMR][1000 genomes] |
rs6674248 | 0.83[AMR][1000 genomes] |
rs6683669 | 0.83[EUR][1000 genomes] |
rs72669891 | 0.83[AMR][1000 genomes] |
rs72672226 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs72672238 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs72672239 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs72672249 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs72672286 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72672292 | 0.83[EUR][1000 genomes] |
rs72674118 | 1.00[EUR][1000 genomes] |
rs72674121 | 1.00[EUR][1000 genomes] |
rs72674127 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1003930 | chr1:58930444-59157038 | Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No data |