Variant report
Variant | rs2840995 |
---|---|
Chromosome Location | chr6:56055928-56055929 |
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] |
---|---|
rs1012257 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1022539 | 0.93[ASN][1000 genomes] |
rs1033478 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12190324 | 0.93[ASN][1000 genomes] |
rs12199712 | 0.93[ASN][1000 genomes] |
rs12199742 | 0.93[ASN][1000 genomes] |
rs1319111 | 0.93[ASN][1000 genomes] |
rs1319112 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs13193925 | 0.91[ASN][1000 genomes] |
rs13209836 | 0.93[ASN][1000 genomes] |
rs1925138 | 0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1925139 | 0.93[ASN][1000 genomes] |
rs1925141 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1925143 | 0.93[ASN][1000 genomes] |
rs1925144 | 0.93[ASN][1000 genomes] |
rs1925147 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1925149 | 0.83[ASN][1000 genomes] |
rs1925179 | 0.93[ASN][1000 genomes] |
rs1925180 | 0.91[ASN][1000 genomes] |
rs1925181 | 0.93[ASN][1000 genomes] |
rs1925185 | 0.91[ASN][1000 genomes] |
rs1925186 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1925189 | 0.93[ASN][1000 genomes] |
rs1980487 | 0.93[ASN][1000 genomes] |
rs2038149 | 0.93[ASN][1000 genomes] |
rs2328675 | 0.96[ASN][1000 genomes] |
rs2328677 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2397204 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2397206 | 0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2397208 | 0.93[ASN][1000 genomes] |
rs2397209 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2745369 | 0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2764052 | 0.85[ASN][1000 genomes] |
rs2764055 | 0.82[ASN][1000 genomes] |
rs2764056 | 0.82[ASN][1000 genomes] |
rs2841000 | 0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2841007 | 0.85[ASN][1000 genomes] |
rs2876630 | 0.93[ASN][1000 genomes] |
rs3846920 | 0.85[ASN][1000 genomes] |
rs3846921 | 0.84[EUR][1000 genomes] |
rs3846922 | 0.93[ASN][1000 genomes] |
rs3846923 | 0.93[ASN][1000 genomes] |
rs3846924 | 0.90[ASN][1000 genomes] |
rs3846925 | 0.90[ASN][1000 genomes] |
rs3857611 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs3857612 | 0.90[ASN][1000 genomes] |
rs4119567 | 0.96[ASN][1000 genomes] |
rs4126555 | 0.93[ASN][1000 genomes] |
rs4126556 | 0.93[ASN][1000 genomes] |
rs4126557 | 0.93[ASN][1000 genomes] |
rs4126558 | 0.93[ASN][1000 genomes] |
rs4140573 | 0.93[ASN][1000 genomes] |
rs4490668 | 0.96[ASN][1000 genomes] |
rs4495274 | 0.96[ASN][1000 genomes] |
rs4554321 | 0.90[ASN][1000 genomes] |
rs4607420 | 0.91[ASN][1000 genomes] |
rs4712113 | 0.91[ASN][1000 genomes] |
rs4715585 | 0.93[ASN][1000 genomes] |
rs4715588 | 0.96[ASN][1000 genomes] |
rs4715589 | 0.93[ASN][1000 genomes] |
rs4715591 | 0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4715592 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4715593 | 0.93[ASN][1000 genomes] |
rs4715597 | 0.89[EUR][1000 genomes] |
rs6459128 | 0.93[ASN][1000 genomes] |
rs6459129 | 0.96[ASN][1000 genomes] |
rs6459133 | 0.96[ASN][1000 genomes] |
rs6459134 | 0.96[ASN][1000 genomes] |
rs6459136 | 0.93[ASN][1000 genomes] |
rs6904431 | 0.93[ASN][1000 genomes] |
rs6904899 | 0.93[ASN][1000 genomes] |
rs6908195 | 0.93[ASN][1000 genomes] |
rs6911907 | 0.93[ASN][1000 genomes] |
rs6914495 | 0.93[ASN][1000 genomes] |
rs6914892 | 0.93[ASN][1000 genomes] |
rs6917593 | 0.91[ASN][1000 genomes] |
rs6922057 | 0.91[ASN][1000 genomes] |
rs6933151 | 0.93[ASN][1000 genomes] |
rs6934945 | 0.87[ASN][1000 genomes] |
rs6935152 | 0.93[ASN][1000 genomes] |
rs6935200 | 0.93[ASN][1000 genomes] |
rs6939465 | 0.93[ASN][1000 genomes] |
rs6939632 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7450147 | 0.93[ASN][1000 genomes] |
rs7754787 | 0.93[ASN][1000 genomes] |
rs7762422 | 0.92[ASN][1000 genomes] |
rs7774374 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9296830 | 0.91[ASN][1000 genomes] |
rs9357891 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9357892 | 0.89[ASN][1000 genomes] |
rs9357894 | 0.82[ASN][1000 genomes] |
rs9370485 | 0.91[ASN][1000 genomes] |
rs9370486 | 0.93[ASN][1000 genomes] |
rs9370493 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9382583 | 0.83[EUR][1000 genomes] |
rs9382595 | 0.93[ASN][1000 genomes] |
rs9396176 | 0.91[ASN][1000 genomes] |
rs9396181 | 0.93[ASN][1000 genomes] |
rs9464348 | 0.93[ASN][1000 genomes] |
rs9475593 | 0.93[ASN][1000 genomes] |
rs9475621 | 0.93[ASN][1000 genomes] |
rs994667 | 0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1034037 | chr6:55222409-56069600 | Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | nsv885911 | chr6:55789704-56143231 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:56053400-56058600 | Weak transcription | Muscle Satellite Cultured Cells | -- |
2 | chr6:56055400-56058600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |