Variant report
Variant | rs2350803 |
---|---|
Chromosome Location | chr2:50132801-50132802 |
allele | G/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] |
---|---|
rs1013597 | 0.82[ASN][1000 genomes] |
rs10495987 | 0.88[EUR][1000 genomes] |
rs11125278 | 0.81[ASN][1000 genomes] |
rs11885824 | 0.85[ASN][1000 genomes] |
rs11902804 | 0.81[ASN][1000 genomes] |
rs12465974 | 0.92[EUR][1000 genomes] |
rs12617277 | 0.85[ASN][1000 genomes] |
rs13007882 | 0.85[ASN][1000 genomes] |
rs13016321 | 0.81[ASN][1000 genomes] |
rs13016900 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13022108 | 0.82[ASN][1000 genomes] |
rs17039448 | 0.81[ASN][1000 genomes] |
rs17039456 | 0.82[ASN][1000 genomes] |
rs17039472 | 0.82[ASN][1000 genomes] |
rs17039484 | 0.85[ASN][1000 genomes] |
rs17039508 | 0.80[ASN][1000 genomes] |
rs2241750 | 0.85[ASN][1000 genomes] |
rs2241752 | 0.82[ASN][1000 genomes] |
rs35373906 | 0.82[ASN][1000 genomes] |
rs4143112 | 0.85[ASN][1000 genomes] |
rs57936567 | 0.84[ASN][1000 genomes] |
rs59672611 | 0.80[ASN][1000 genomes] |
rs60884569 | 0.84[ASN][1000 genomes] |
rs62132409 | 0.84[ASN][1000 genomes] |
rs62132414 | 0.82[ASN][1000 genomes] |
rs6545136 | 0.89[EUR][1000 genomes] |
rs6758043 | 0.85[ASN][1000 genomes] |
rs6758276 | 0.85[ASN][1000 genomes] |
rs7598993 | 0.82[ASN][1000 genomes] |
rs920033 | 0.84[ASN][1000 genomes] |
rs920034 | 0.85[ASN][1000 genomes] |
rs920035 | 0.85[ASN][1000 genomes] |
rs971732 | 0.93[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3388948 | chr2:50092667-50602681 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
2 | esv3399511 | chr2:50092687-50602651 | Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:50131000-50137000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
2 | chr2:50132200-50134800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |