Variant report
Variant | rs669503 |
---|---|
Chromosome Location | chr12:10983074-10983075 |
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] |
---|---|
rs10743927 | 0.87[EUR][1000 genomes] |
rs10845220 | 0.87[EUR][1000 genomes] |
rs1548804 | 0.90[EUR][1000 genomes] |
rs2159899 | 0.90[EUR][1000 genomes] |
rs2232956 | 0.83[EUR][1000 genomes] |
rs2418105 | 0.83[EUR][1000 genomes] |
rs2418106 | 0.90[EUR][1000 genomes] |
rs2900550 | 0.83[EUR][1000 genomes] |
rs3851578 | 0.83[EUR][1000 genomes] |
rs3906864 | 0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs612808 | 0.90[EUR][1000 genomes] |
rs619381 | 0.85[EUR][1000 genomes] |
rs621112 | 0.83[EUR][1000 genomes] |
rs6488328 | 0.83[EUR][1000 genomes] |
rs666841 | 0.83[EUR][1000 genomes] |
rs667128 | 0.85[EUR][1000 genomes] |
rs684208 | 0.80[EUR][1000 genomes] |
rs7299578 | 0.83[EUR][1000 genomes] |
rs741092 | 0.90[EUR][1000 genomes] |
rs763839 | 0.87[EUR][1000 genomes] |
rs7957888 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1049362 | chr12:10893573-11018850 | Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv898776 | chr12:10909412-11032045 | Genic enhancers Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | esv2758294 | chr12:10969620-11714921 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 52 gene(s) | inside rSNPs | diseases |
4 | esv2759879 | chr12:10969620-11714921 | Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 52 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs669503 | PRR4 | cis | parietal | SCAN |
rs669503 | TAS2R8 | cis | parietal | SCAN |
rs669503 | TAS2R43 | cis | cerebellum | SCAN |
rs669503 | TAS2R43 | cis | parietal | SCAN |
rs669503 | TAS2R13 | cis | cerebellum | SCAN |
rs669503 | TAS2R10 | cis | parietal | SCAN |
rs669503 | TAS2R9 | cis | parietal | SCAN |
rs669503 | TAS2R45 | N/A | lymphoblastoid | RTeQTL |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:10973600-11009600 | Weak transcription | HSMM | muscle |