Variant report
Variant | rs8048383 |
---|---|
Chromosome Location | chr16:64950482-64950483 |
allele | A/C |
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] |
---|---|
rs1025311 | 0.85[ASN][1000 genomes] |
rs1079008 | 0.83[ASN][1000 genomes] |
rs12445593 | 0.96[ASN][1000 genomes] |
rs12447201 | 0.80[ASN][1000 genomes] |
rs12597529 | 0.89[ASN][1000 genomes] |
rs12925954 | 0.85[ASN][1000 genomes] |
rs12926007 | 0.98[ASN][1000 genomes] |
rs12935145 | 0.81[ASN][1000 genomes] |
rs1520230 | 0.82[ASN][1000 genomes] |
rs1520231 | 0.81[ASN][1000 genomes] |
rs1520234 | 0.81[ASN][1000 genomes] |
rs1520241 | 0.89[ASN][1000 genomes] |
rs1520243 | 0.82[ASN][1000 genomes] |
rs16942779 | 0.99[ASN][1000 genomes] |
rs16968098 | 0.99[ASN][1000 genomes] |
rs16968101 | 0.99[ASN][1000 genomes] |
rs16968102 | 0.99[ASN][1000 genomes] |
rs1850966 | 0.82[ASN][1000 genomes] |
rs185394 | 0.94[ASN][1000 genomes] |
rs1874457 | 0.81[ASN][1000 genomes] |
rs1874458 | 0.81[ASN][1000 genomes] |
rs1874459 | 0.81[ASN][1000 genomes] |
rs1879260 | 0.81[ASN][1000 genomes] |
rs1896755 | 0.99[ASN][1000 genomes] |
rs1896756 | 0.99[ASN][1000 genomes] |
rs1908723 | 0.81[ASN][1000 genomes] |
rs2115393 | 0.95[ASN][1000 genomes] |
rs2280396 | 0.82[ASN][1000 genomes] |
rs257335 | 0.82[ASN][1000 genomes] |
rs257336 | 0.82[ASN][1000 genomes] |
rs257337 | 0.80[ASN][1000 genomes] |
rs257341 | 0.90[ASN][1000 genomes] |
rs257487 | 0.82[ASN][1000 genomes] |
rs257490 | 0.82[ASN][1000 genomes] |
rs257497 | 0.90[ASN][1000 genomes] |
rs257498 | 0.90[ASN][1000 genomes] |
rs257499 | 0.92[ASN][1000 genomes] |
rs28216 | 0.84[ASN][1000 genomes] |
rs34699531 | 0.99[ASN][1000 genomes] |
rs34893901 | 0.97[ASN][1000 genomes] |
rs35139 | 0.90[ASN][1000 genomes] |
rs35140 | 0.90[ASN][1000 genomes] |
rs35144 | 0.92[ASN][1000 genomes] |
rs35145 | 0.92[ASN][1000 genomes] |
rs35146 | 0.92[ASN][1000 genomes] |
rs35148 | 0.91[ASN][1000 genomes] |
rs35149 | 0.94[ASN][1000 genomes] |
rs35150 | 0.94[ASN][1000 genomes] |
rs35152 | 0.94[ASN][1000 genomes] |
rs35154 | 0.94[ASN][1000 genomes] |
rs35155 | 0.94[ASN][1000 genomes] |
rs35156 | 0.94[ASN][1000 genomes] |
rs35157 | 0.93[ASN][1000 genomes] |
rs35158 | 0.93[ASN][1000 genomes] |
rs35159 | 0.93[ASN][1000 genomes] |
rs35160 | 0.93[ASN][1000 genomes] |
rs35161 | 0.93[ASN][1000 genomes] |
rs35162 | 0.93[ASN][1000 genomes] |
rs35163 | 0.94[ASN][1000 genomes] |
rs35164 | 0.94[ASN][1000 genomes] |
rs35165 | 0.91[ASN][1000 genomes] |
rs35166 | 0.94[ASN][1000 genomes] |
rs35167 | 0.94[ASN][1000 genomes] |
rs35169 | 0.94[ASN][1000 genomes] |
rs35170 | 0.94[ASN][1000 genomes] |
rs35171 | 0.94[ASN][1000 genomes] |
rs35176 | 0.82[ASN][1000 genomes] |
rs35177 | 0.81[ASN][1000 genomes] |
rs35178 | 0.85[ASN][1000 genomes] |
rs35179 | 0.85[ASN][1000 genomes] |
rs35180 | 0.84[ASN][1000 genomes] |
rs35188 | 0.83[ASN][1000 genomes] |
rs35191 | 0.84[ASN][1000 genomes] |
rs35192 | 0.84[ASN][1000 genomes] |
rs35193 | 0.82[ASN][1000 genomes] |
rs35195 | 0.84[ASN][1000 genomes] |
rs35198 | 0.84[ASN][1000 genomes] |
rs35199 | 0.84[ASN][1000 genomes] |
rs35200 | 0.84[ASN][1000 genomes] |
rs35203 | 0.83[ASN][1000 genomes] |
rs35204 | 0.84[ASN][1000 genomes] |
rs35205 | 0.84[ASN][1000 genomes] |
rs35206 | 0.84[ASN][1000 genomes] |
rs35208 | 0.84[ASN][1000 genomes] |
rs35209 | 0.83[ASN][1000 genomes] |
rs35210 | 0.82[ASN][1000 genomes] |
rs35214 | 0.84[ASN][1000 genomes] |
rs35215 | 0.84[ASN][1000 genomes] |
rs35216 | 0.84[ASN][1000 genomes] |
rs35218 | 0.84[ASN][1000 genomes] |
rs35219 | 0.86[ASN][1000 genomes] |
rs35224 | 0.86[ASN][1000 genomes] |
rs35226 | 0.83[ASN][1000 genomes] |
rs35263777 | 0.83[ASN][1000 genomes] |
rs35557609 | 0.99[ASN][1000 genomes] |
rs35891857 | 0.99[ASN][1000 genomes] |
rs369499 | 0.94[ASN][1000 genomes] |
rs382418 | 0.94[ASN][1000 genomes] |
rs385317 | 0.99[ASN][1000 genomes] |
rs388039 | 0.94[ASN][1000 genomes] |
rs396950 | 0.94[ASN][1000 genomes] |
rs400182 | 0.94[ASN][1000 genomes] |
rs40113 | 0.94[ASN][1000 genomes] |
rs40115 | 0.83[ASN][1000 genomes] |
rs40116 | 0.84[ASN][1000 genomes] |
rs40510 | 0.94[ASN][1000 genomes] |
rs406925 | 0.94[ASN][1000 genomes] |
rs408330 | 0.99[ASN][1000 genomes] |
rs422274 | 0.94[ASN][1000 genomes] |
rs42863 | 0.84[ASN][1000 genomes] |
rs436962 | 0.98[ASN][1000 genomes] |
rs437402 | 0.94[ASN][1000 genomes] |
rs437408 | 0.94[ASN][1000 genomes] |
rs447096 | 0.94[ASN][1000 genomes] |
rs453866 | 0.96[ASN][1000 genomes] |
rs462735 | 0.90[ASN][1000 genomes] |
rs4967858 | 0.99[ASN][1000 genomes] |
rs4967859 | 0.99[ASN][1000 genomes] |
rs4967860 | 0.99[ASN][1000 genomes] |
rs4967861 | 0.99[ASN][1000 genomes] |
rs4967862 | 0.99[ASN][1000 genomes] |
rs4967866 | 0.89[ASN][1000 genomes] |
rs4967875 | 0.99[ASN][1000 genomes] |
rs4967876 | 0.99[ASN][1000 genomes] |
rs4967882 | 0.82[ASN][1000 genomes] |
rs610896 | 0.99[ASN][1000 genomes] |
rs611241 | 0.99[ASN][1000 genomes] |
rs611322 | 0.99[ASN][1000 genomes] |
rs62042237 | 0.82[ASN][1000 genomes] |
rs7188339 | 0.97[ASN][1000 genomes] |
rs7189660 | 0.97[ASN][1000 genomes] |
rs878359 | 0.82[ASN][1000 genomes] |
rs909003 | 0.82[ASN][1000 genomes] |
rs973200 | 0.87[ASN][1000 genomes] |
rs988878 | 0.81[AFR][1000 genomes] |
rs990639 | 0.82[ASN][1000 genomes] |
rs9935608 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948640 | chr16:64859061-65112790 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
2 | nsv984501 | chr16:64919797-64993897 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive regionmiRNA target site | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:64945000-64954400 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
2 | chr16:64950000-64952000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |