Variant report
Variant | rs7635610 |
---|---|
Chromosome Location | chr3:156097672-156097673 |
allele | A/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 | chr3:156096464..156098715-chr3:156098972..156101153,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12163648 | 1.00[EUR][1000 genomes] |
rs13315734 | 1.00[EUR][1000 genomes] |
rs13323310 | 1.00[EUR][1000 genomes] |
rs13327461 | 1.00[EUR][1000 genomes] |
rs1375929 | 1.00[EUR][1000 genomes] |
rs16825997 | 1.00[EUR][1000 genomes] |
rs16826014 | 1.00[EUR][1000 genomes] |
rs16826015 | 1.00[EUR][1000 genomes] |
rs16826037 | 0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16826126 | 1.00[EUR][1000 genomes] |
rs16826244 | 1.00[EUR][1000 genomes] |
rs16826248 | 1.00[EUR][1000 genomes] |
rs16826250 | 1.00[EUR][1000 genomes] |
rs16826264 | 1.00[EUR][1000 genomes] |
rs28368547 | 1.00[EUR][1000 genomes] |
rs3755629 | 0.85[YRI][hapmap] |
rs4630897 | 1.00[EUR][1000 genomes] |
rs4989481 | 0.81[YRI][hapmap] |
rs55973260 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57058377 | 1.00[EUR][1000 genomes] |
rs58463289 | 1.00[EUR][1000 genomes] |
rs59046488 | 1.00[EUR][1000 genomes] |
rs59223796 | 1.00[EUR][1000 genomes] |
rs60249133 | 1.00[EUR][1000 genomes] |
rs61458860 | 1.00[EUR][1000 genomes] |
rs6441060 | 1.00[EUR][1000 genomes] |
rs6441062 | 0.83[AMR][1000 genomes] |
rs6441071 | 1.00[EUR][1000 genomes] |
rs6441073 | 1.00[EUR][1000 genomes] |
rs6762484 | 1.00[EUR][1000 genomes] |
rs6764802 | 1.00[EUR][1000 genomes] |
rs6765899 | 1.00[MEX][hapmap];1.00[EUR][1000 genomes] |
rs6771705 | 1.00[EUR][1000 genomes] |
rs6773597 | 1.00[EUR][1000 genomes] |
rs6775545 | 0.83[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6794030 | 1.00[EUR][1000 genomes] |
rs6806552 | 0.94[ASW][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.90[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73014109 | 1.00[EUR][1000 genomes] |
rs73014142 | 1.00[EUR][1000 genomes] |
rs73014146 | 1.00[EUR][1000 genomes] |
rs73014153 | 1.00[EUR][1000 genomes] |
rs73014154 | 1.00[EUR][1000 genomes] |
rs73014161 | 1.00[EUR][1000 genomes] |
rs73016002 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73017905 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73017919 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73017930 | 1.00[EUR][1000 genomes] |
rs73017998 | 1.00[EUR][1000 genomes] |
rs73019918 | 1.00[EUR][1000 genomes] |
rs73019921 | 1.00[EUR][1000 genomes] |
rs73019934 | 1.00[EUR][1000 genomes] |
rs73019935 | 1.00[EUR][1000 genomes] |
rs73019940 | 1.00[EUR][1000 genomes] |
rs73873328 | 0.83[AMR][1000 genomes] |
rs73873329 | 0.83[AMR][1000 genomes] |
rs7621244 | 1.00[EUR][1000 genomes] |
rs7625905 | 1.00[EUR][1000 genomes] |
rs7626513 | 1.00[EUR][1000 genomes] |
rs7634841 | 0.84[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7639374 | 1.00[EUR][1000 genomes] |
rs7641812 | 1.00[EUR][1000 genomes] |
rs7648151 | 1.00[EUR][1000 genomes] |
rs7648434 | 1.00[EUR][1000 genomes] |
rs924352 | 1.00[EUR][1000 genomes] |
rs9289963 | 1.00[EUR][1000 genomes] |
rs9289964 | 1.00[EUR][1000 genomes] |
rs9810962 | 1.00[EUR][1000 genomes] |
rs9812993 | 1.00[EUR][1000 genomes] |
rs9823622 | 0.83[AMR][1000 genomes] |
rs9828203 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9829670 | 1.00[EUR][1000 genomes] |
rs9830004 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9833026 | 1.00[EUR][1000 genomes] |
rs9833563 | 1.00[EUR][1000 genomes] |
rs9839152 | 0.89[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9844410 | 0.83[AMR][1000 genomes] |
rs9846546 | 0.83[YRI][hapmap] |
rs9850840 | 0.82[YRI][hapmap] |
rs9853634 | 0.83[YRI][hapmap] |
rs9855009 | 1.00[MEX][hapmap];0.83[AMR][1000 genomes] |
rs9858999 | 1.00[EUR][1000 genomes] |
rs9866817 | 1.00[EUR][1000 genomes] |
rs9867561 | 0.83[AMR][1000 genomes] |
rs9872444 | 0.83[AMR][1000 genomes] |
rs9873235 | 1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9874012 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9877749 | 1.00[EUR][1000 genomes] |
rs9880939 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014755 | chr3:155889430-156411894 | Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
2 | esv1809143 | chr3:156092164-156098920 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv592115 | chr3:156092548-156097836 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | esv1806015 | chr3:156095513-156114898 | Weak transcription Enhancers Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:156090800-156100600 | Weak transcription | Fetal Muscle Leg | muscle |
2 | chr3:156092400-156101600 | Weak transcription | Aorta | Aorta |
3 | chr3:156094200-156105000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr3:156097400-156098000 | Enhancers | Gastric | stomach |
5 | chr3:156097600-156097800 | Enhancers | Pancreatic Islets | Pancreatic Islet |