Variant report
Variant | rs12708346 |
---|---|
Chromosome Location | chr11:34422351-34422352 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000220204 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10768074 | 0.85[ASN][1000 genomes] |
rs10836210 | 0.88[ASN][1000 genomes] |
rs10836212 | 1.00[ASN][1000 genomes] |
rs10836213 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10836214 | 1.00[ASN][1000 genomes] |
rs10836219 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10836220 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10836221 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10836226 | 0.85[ASN][1000 genomes] |
rs10836227 | 0.85[ASN][1000 genomes] |
rs10836228 | 0.85[ASN][1000 genomes] |
rs10836231 | 0.81[ASN][1000 genomes] |
rs10836232 | 0.82[ASN][1000 genomes] |
rs10836233 | 0.82[ASN][1000 genomes] |
rs10836235 | 0.82[ASN][1000 genomes] |
rs11032650 | 0.84[ASN][1000 genomes] |
rs11032677 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11032685 | 0.85[ASN][1000 genomes] |
rs11032686 | 0.85[ASN][1000 genomes] |
rs11032687 | 0.85[ASN][1000 genomes] |
rs11032688 | 0.85[ASN][1000 genomes] |
rs11032689 | 0.81[ASN][1000 genomes] |
rs11032690 | 0.85[ASN][1000 genomes] |
rs11032691 | 0.85[ASN][1000 genomes] |
rs11032692 | 0.85[ASN][1000 genomes] |
rs11032693 | 0.84[ASN][1000 genomes] |
rs11032694 | 0.84[ASN][1000 genomes] |
rs11032697 | 0.82[ASN][1000 genomes] |
rs11032701 | 0.82[ASN][1000 genomes] |
rs11605706 | 0.97[ASN][1000 genomes] |
rs12276378 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12277763 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12285367 | 0.85[ASN][1000 genomes] |
rs12289239 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12292102 | 0.85[ASN][1000 genomes] |
rs12786782 | 0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12802066 | 0.85[ASN][1000 genomes] |
rs1408034 | 0.82[ASN][1000 genomes] |
rs1408036 | 0.80[ASN][1000 genomes] |
rs1408037 | 0.81[ASN][1000 genomes] |
rs1408038 | 0.85[ASN][1000 genomes] |
rs1408039 | 0.85[ASN][1000 genomes] |
rs1408040 | 0.85[ASN][1000 genomes] |
rs17884666 | 0.80[ASN][1000 genomes] |
rs17885743 | 0.82[ASN][1000 genomes] |
rs2073059 | 0.82[ASN][1000 genomes] |
rs2223676 | 0.81[ASN][1000 genomes] |
rs34682777 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3758730 | 0.82[ASN][1000 genomes] |
rs5028597 | 0.87[EUR][1000 genomes] |
rs60077297 | 0.85[ASN][1000 genomes] |
rs61447308 | 0.85[ASN][1000 genomes] |
rs6484720 | 0.81[ASN][1000 genomes] |
rs6484721 | 0.81[ASN][1000 genomes] |
rs7111687 | 0.82[ASN][1000 genomes] |
rs7111765 | 0.84[ASN][1000 genomes] |
rs7111903 | 0.82[ASN][1000 genomes] |
rs7115206 | 0.82[ASN][1000 genomes] |
rs7117540 | 0.81[ASN][1000 genomes] |
rs7127109 | 0.81[ASN][1000 genomes] |
rs7127314 | 0.81[ASN][1000 genomes] |
rs7127560 | 0.81[ASN][1000 genomes] |
rs7128380 | 1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7131159 | 0.81[ASN][1000 genomes] |
rs7131473 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7928156 | 0.81[ASN][1000 genomes] |
rs7928368 | 1.00[ASN][1000 genomes] |
rs7928635 | 1.00[ASN][1000 genomes] |
rs7929333 | 0.85[ASN][1000 genomes] |
rs7929460 | 0.81[ASN][1000 genomes] |
rs7929574 | 0.85[ASN][1000 genomes] |
rs7929899 | 0.85[ASN][1000 genomes] |
rs7929931 | 0.85[ASN][1000 genomes] |
rs7929952 | 0.85[ASN][1000 genomes] |
rs7930070 | 0.85[ASN][1000 genomes] |
rs7944397 | 0.81[ASN][1000 genomes] |
rs9651597 | 0.84[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv897205 | chr11:34248229-34507213 | Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv897207 | chr11:34253683-34621004 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
3 | nsv897208 | chr11:34257064-34562247 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
4 | nsv897209 | chr11:34309519-34548906 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
5 | nsv983151 | chr11:34401342-34444667 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:34419000-34428600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr11:34421600-34422400 | ZNF genes & repeats | Foreskin Fibroblast Primary Cells skin01 | Skin |