Variant report
Variant | rs4372623 |
---|---|
Chromosome Location | chr14:84752238-84752239 |
allele | C/T |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr14:84751809..84754653-chr14:84755331..84758306,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10129851 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10132898 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10134005 | 0.97[ASN][1000 genomes] |
rs10145673 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10148642 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs10150745 | 0.96[ASN][1000 genomes] |
rs12436486 | 0.92[EUR][1000 genomes] |
rs17707121 | 0.92[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs28399118 | 0.98[ASN][1000 genomes] |
rs28446157 | 0.98[ASN][1000 genomes] |
rs3924602 | 0.93[EUR][1000 genomes] |
rs3935697 | 0.98[ASN][1000 genomes] |
rs4277275 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55986944 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7142508 | 0.96[ASN][1000 genomes] |
rs7143199 | 0.96[ASN][1000 genomes] |
rs7154367 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7157365 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7157373 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs8005901 | 0.98[ASN][1000 genomes] |
rs8009583 | 0.98[ASN][1000 genomes] |
rs8012329 | 0.96[ASN][1000 genomes] |
rs8019836 | 0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv902161 | chr14:84699866-84769903 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
2 | nsv832845 | chr14:84726378-84900199 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:84751600-84752400 | Enhancers | Adipose Nuclei | Adipose |