Variant report
Variant | rs1380065 |
---|---|
Chromosome Location | chr4:56028966-56028967 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:56023096..56025181-chr4:56027866..56029922,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10011355 | 1.00[AMR][1000 genomes] |
rs10027862 | 1.00[AMR][1000 genomes] |
rs10028745 | 1.00[AMR][1000 genomes] |
rs1158370 | 1.00[AMR][1000 genomes] |
rs12716019 | 1.00[AMR][1000 genomes] |
rs1380070 | 1.00[AMR][1000 genomes] |
rs1458821 | 1.00[AMR][1000 genomes] |
rs1543930 | 1.00[AMR][1000 genomes] |
rs1543931 | 1.00[AMR][1000 genomes] |
rs1551639 | 1.00[AMR][1000 genomes] |
rs1870380 | 1.00[AMR][1000 genomes] |
rs1968771 | 1.00[AMR][1000 genomes] |
rs2168946 | 1.00[AMR][1000 genomes] |
rs2412636 | 1.00[AMR][1000 genomes] |
rs4352535 | 1.00[AMR][1000 genomes] |
rs57190330 | 1.00[AMR][1000 genomes] |
rs59384774 | 1.00[AMR][1000 genomes] |
rs6554250 | 1.00[AMR][1000 genomes] |
rs6824124 | 1.00[AMR][1000 genomes] |
rs6826761 | 1.00[AMR][1000 genomes] |
rs6835605 | 1.00[AMR][1000 genomes] |
rs6855258 | 1.00[AMR][1000 genomes] |
rs6857669 | 1.00[AMR][1000 genomes] |
rs7666097 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv526344 | chr4:55522488-56231119 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:56027400-56029800 | Weak transcription | HUVEC | blood vessel |