Variant report
Variant | rs245283 |
---|---|
Chromosome Location | chr5:57632039-57632040 |
allele | A/T |
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 | chr5:57631449..57633354-chr5:57753923..57756596,2 | MCF-7 | breast: | |
2 | chr5:57626348..57628340-chr5:57631226..57633135,2 | MCF-7 | breast: | |
3 | chr5:57631529..57633714-chr5:57748489..57751374,2 | MCF-7 | breast: | |
4 | chr5:57626809..57628969-chr5:57631337..57632977,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000145632 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs151865 | 0.94[EUR][1000 genomes] |
rs151869 | 1.00[ASN][1000 genomes] |
rs151870 | 0.94[EUR][1000 genomes] |
rs154672 | 1.00[ASN][1000 genomes] |
rs154674 | 1.00[ASN][1000 genomes] |
rs168652 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs173448 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs181749 | 0.90[EUR][1000 genomes] |
rs193497 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs245281 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs245284 | 0.96[EUR][1000 genomes] |
rs245286 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs245465 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs245466 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs245467 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs245468 | 0.90[EUR][1000 genomes] |
rs245469 | 0.86[EUR][1000 genomes] |
rs26970 | 0.83[EUR][1000 genomes] |
rs26971 | 0.83[EUR][1000 genomes] |
rs26972 | 0.83[EUR][1000 genomes] |
rs26973 | 0.83[EUR][1000 genomes] |
rs27568 | 0.83[EUR][1000 genomes] |
rs32629 | 0.83[EUR][1000 genomes] |
rs36610 | 1.00[ASN][1000 genomes] |
rs36646 | 0.86[EUR][1000 genomes] |
rs36647 | 0.86[EUR][1000 genomes] |
rs393809 | 0.84[EUR][1000 genomes] |
rs40622 | 0.86[EUR][1000 genomes] |
rs41234 | 0.98[ASN][1000 genomes] |
rs420498 | 0.84[EUR][1000 genomes] |
rs42317 | 0.86[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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:57627200-57634000 | Weak transcription | Aorta | Aorta |
2 | chr5:57630400-57634600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |