Variant report
Variant | rs59254378 |
---|---|
Chromosome Location | chr12:60581477-60581478 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1021886 | 0.85[EUR][1000 genomes] |
rs10784049 | 0.85[EUR][1000 genomes] |
rs12312951 | 0.85[EUR][1000 genomes] |
rs12313027 | 0.85[EUR][1000 genomes] |
rs1394329 | 0.85[EUR][1000 genomes] |
rs1466939 | 0.85[EUR][1000 genomes] |
rs1504461 | 0.85[EUR][1000 genomes] |
rs1587822 | 0.85[EUR][1000 genomes] |
rs1587823 | 0.85[EUR][1000 genomes] |
rs1604863 | 0.85[EUR][1000 genomes] |
rs1604864 | 0.85[EUR][1000 genomes] |
rs17123432 | 1.00[EUR][1000 genomes] |
rs17123453 | 1.00[EUR][1000 genomes] |
rs17123464 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs17123473 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17123496 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17123529 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17123574 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1827639 | 0.85[EUR][1000 genomes] |
rs1827640 | 0.85[EUR][1000 genomes] |
rs1910676 | 0.85[EUR][1000 genomes] |
rs1960370 | 0.85[EUR][1000 genomes] |
rs1961693 | 0.85[EUR][1000 genomes] |
rs1967225 | 0.85[EUR][1000 genomes] |
rs1995517 | 0.85[EUR][1000 genomes] |
rs2089152 | 0.85[EUR][1000 genomes] |
rs2089153 | 0.85[EUR][1000 genomes] |
rs2102256 | 0.85[EUR][1000 genomes] |
rs2134884 | 0.85[EUR][1000 genomes] |
rs2134885 | 0.85[EUR][1000 genomes] |
rs2134886 | 0.85[EUR][1000 genomes] |
rs2202361 | 0.85[EUR][1000 genomes] |
rs2202362 | 0.85[EUR][1000 genomes] |
rs2202363 | 0.85[EUR][1000 genomes] |
rs2202364 | 0.85[EUR][1000 genomes] |
rs2262938 | 0.85[EUR][1000 genomes] |
rs2262940 | 0.85[EUR][1000 genomes] |
rs2363586 | 0.85[EUR][1000 genomes] |
rs2363588 | 0.85[EUR][1000 genomes] |
rs2455997 | 0.85[EUR][1000 genomes] |
rs2468380 | 0.85[EUR][1000 genomes] |
rs2468381 | 0.85[EUR][1000 genomes] |
rs2655849 | 0.85[EUR][1000 genomes] |
rs2655850 | 0.85[EUR][1000 genomes] |
rs2655851 | 0.85[EUR][1000 genomes] |
rs2655854 | 0.85[EUR][1000 genomes] |
rs2655855 | 0.85[EUR][1000 genomes] |
rs2655862 | 0.85[EUR][1000 genomes] |
rs2655863 | 0.85[EUR][1000 genomes] |
rs2655864 | 0.85[EUR][1000 genomes] |
rs2655865 | 0.85[EUR][1000 genomes] |
rs2655866 | 0.85[EUR][1000 genomes] |
rs2655867 | 0.85[EUR][1000 genomes] |
rs2655881 | 0.85[EUR][1000 genomes] |
rs2655882 | 0.85[EUR][1000 genomes] |
rs2655883 | 0.85[EUR][1000 genomes] |
rs2731450 | 0.85[EUR][1000 genomes] |
rs2731452 | 0.85[EUR][1000 genomes] |
rs2731453 | 0.85[EUR][1000 genomes] |
rs2731454 | 0.85[EUR][1000 genomes] |
rs2731478 | 0.85[EUR][1000 genomes] |
rs2731479 | 0.85[EUR][1000 genomes] |
rs2731480 | 0.85[EUR][1000 genomes] |
rs2731483 | 0.85[EUR][1000 genomes] |
rs2731486 | 0.85[EUR][1000 genomes] |
rs2731489 | 0.85[EUR][1000 genomes] |
rs2731493 | 0.85[EUR][1000 genomes] |
rs2731496 | 0.85[EUR][1000 genomes] |
rs2938648 | 0.85[EUR][1000 genomes] |
rs3912929 | 1.00[EUR][1000 genomes] |
rs4500518 | 0.85[EUR][1000 genomes] |
rs55897976 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56145591 | 0.93[EUR][1000 genomes] |
rs56739047 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59465291 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60106464 | 1.00[EUR][1000 genomes] |
rs60652670 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6581317 | 0.85[EUR][1000 genomes] |
rs7307145 | 0.85[EUR][1000 genomes] |
rs73363801 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs73365606 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs73370714 | 0.93[EUR][1000 genomes] |
rs73370721 | 0.93[EUR][1000 genomes] |
rs73370795 | 0.93[EUR][1000 genomes] |
rs73370797 | 0.93[EUR][1000 genomes] |
rs73370800 | 0.93[EUR][1000 genomes] |
rs74093673 | 1.00[EUR][1000 genomes] |
rs74093676 | 1.00[EUR][1000 genomes] |
rs74096730 | 1.00[EUR][1000 genomes] |
rs74096918 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs74096923 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs74096924 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096934 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096935 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096939 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096943 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096947 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096948 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096953 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74096958 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7965723 | 1.00[EUR][1000 genomes] |
rs7968422 | 0.85[EUR][1000 genomes] |
rs7974290 | 0.85[EUR][1000 genomes] |
rs905724 | 0.85[EUR][1000 genomes] |
rs905725 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428591 | chr12:60446360-60631044 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv899137 | chr12:60568891-60797083 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:60567200-60582400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |