Variant report
Variant | rs26976 |
---|---|
Chromosome Location | chr5:57657705-57657706 |
allele | C/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 | chr5:57656384..57658346-chr5:57754489..57756599,3 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000145632 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs151915 | 0.94[EUR][1000 genomes] |
rs151921 | 0.89[EUR][1000 genomes] |
rs151922 | 0.88[EUR][1000 genomes] |
rs151923 | 0.89[EUR][1000 genomes] |
rs154681 | 0.94[EUR][1000 genomes] |
rs244698 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs244700 | 0.94[EUR][1000 genomes] |
rs2548599 | 0.93[EUR][1000 genomes] |
rs2652499 | 0.92[EUR][1000 genomes] |
rs2662618 | 0.92[EUR][1000 genomes] |
rs26979 | 0.96[EUR][1000 genomes] |
rs27212 | 0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs27604 | 0.96[EUR][1000 genomes] |
rs27917 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs36645 | 0.87[EUR][1000 genomes] |
rs399282 | 0.94[EUR][1000 genomes] |
rs412028 | 0.94[EUR][1000 genomes] |
rs451022 | 0.94[EUR][1000 genomes] |
rs696189 | 0.89[EUR][1000 genomes] |
rs697087 | 0.92[EUR][1000 genomes] |
rs697088 | 0.94[EUR][1000 genomes] |
rs702586 | 0.92[EUR][1000 genomes] |
rs834935 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3489100 | chr5:57545689-57669673 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | esv3489101 | chr5:57545689-57669673 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv4842 | chr5:57653257-57694850 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv3440932 | chr5:57656620-57659168 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:57657000-57661600 | Weak transcription | Fetal Heart | heart |