Variant report
Variant | rs73189389 |
---|---|
Chromosome Location | chr21:17381888-17381889 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr21:17379808..17382152-chr21:17382746..17385605,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs2823548 | 1.00[ASN][1000 genomes] |
rs379332 | 0.90[EUR][1000 genomes] |
rs398068 | 0.82[EUR][1000 genomes] |
rs424868 | 0.90[EUR][1000 genomes] |
rs66771945 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs66837398 | 1.00[ASN][1000 genomes] |
rs67491042 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7280631 | 1.00[ASN][1000 genomes] |
rs73187465 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs73187468 | 0.90[EUR][1000 genomes] |
rs73187483 | 0.92[EUR][1000 genomes] |
rs73187487 | 0.92[EUR][1000 genomes] |
rs73187492 | 0.90[EUR][1000 genomes] |
rs73189356 | 0.92[EUR][1000 genomes] |
rs73189362 | 0.92[EUR][1000 genomes] |
rs73189364 | 0.94[EUR][1000 genomes] |
rs73189378 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73189381 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73189383 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs73189390 | 1.00[ASN][1000 genomes] |
rs73191491 | 0.87[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9981871 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1064664 | chr21:17336936-17405756 | Enhancers Active TSS Flanking Active TSS Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | esv3358532 | chr21:17380631-17382679 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:17380800-17384000 | Weak transcription | Osteobl | bone |