Variant report
Variant | rs9449091 |
---|---|
Chromosome Location | chr6:81308727-81308728 |
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] |
---|---|
rs10943716 | 0.82[EUR][1000 genomes] |
rs10943717 | 0.81[EUR][1000 genomes] |
rs10943718 | 0.81[EUR][1000 genomes] |
rs12200933 | 0.81[EUR][1000 genomes] |
rs1657308 | 0.80[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs1698340 | 0.82[EUR][1000 genomes] |
rs2085110 | 0.85[AMR][1000 genomes] |
rs2168104 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2322840 | 0.82[EUR][1000 genomes] |
rs2322841 | 0.82[EUR][1000 genomes] |
rs2444795 | 0.87[AMR][1000 genomes] |
rs2496682 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2503719 | 0.83[EUR][1000 genomes] |
rs2653481 | 0.82[EUR][1000 genomes] |
rs2917599 | 0.83[EUR][1000 genomes] |
rs2917601 | 0.81[EUR][1000 genomes] |
rs4455626 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs4481396 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs4612123 | 0.82[EUR][1000 genomes] |
rs484019 | 0.82[EUR][1000 genomes] |
rs504505 | 0.83[EUR][1000 genomes] |
rs585401 | 0.82[EUR][1000 genomes] |
rs591403 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs600262 | 0.84[EUR][1000 genomes] |
rs607208 | 0.82[EUR][1000 genomes] |
rs630692 | 0.84[EUR][1000 genomes] |
rs643557 | 0.84[EUR][1000 genomes] |
rs652200 | 0.83[EUR][1000 genomes] |
rs668698 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs676224 | 0.84[EUR][1000 genomes] |
rs7738465 | 0.80[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9443791 | 0.84[EUR][1000 genomes] |
rs9443797 | 0.82[EUR][1000 genomes] |
rs9449059 | 0.82[EUR][1000 genomes] |
rs9449060 | 0.80[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9449061 | 0.82[EUR][1000 genomes] |
rs9449063 | 0.82[EUR][1000 genomes] |
rs9449067 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9449068 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531333 | chr6:81042427-81836484 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv1019670 | chr6:81086504-81569984 | ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
3 | nsv915714 | chr6:81134888-81366749 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv886312 | chr6:81166178-81309481 | Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
5 | nsv1020533 | chr6:81288890-81406533 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv538340 | chr6:81288890-81406533 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv508417 | chr6:81290516-81330590 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv604085 | chr6:81297890-81439973 | Enhancers Weak transcription Flanking Active TSS 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 | chr6:81294800-81317000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |