Variant report
Variant | rs74078240 |
---|---|
Chromosome Location | chr12:42010782-42010783 |
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] |
---|---|
rs10082904 | 1.00[EUR][1000 genomes] |
rs10506199 | 1.00[EUR][1000 genomes] |
rs10506200 | 1.00[EUR][1000 genomes] |
rs17129486 | 1.00[EUR][1000 genomes] |
rs17129531 | 1.00[EUR][1000 genomes] |
rs17129534 | 1.00[EUR][1000 genomes] |
rs17129537 | 1.00[EUR][1000 genomes] |
rs17129541 | 1.00[EUR][1000 genomes] |
rs55724233 | 1.00[EUR][1000 genomes] |
rs55792075 | 1.00[EUR][1000 genomes] |
rs55856507 | 1.00[EUR][1000 genomes] |
rs55884504 | 1.00[EUR][1000 genomes] |
rs55968872 | 1.00[EUR][1000 genomes] |
rs56146127 | 1.00[EUR][1000 genomes] |
rs56185948 | 1.00[EUR][1000 genomes] |
rs56261613 | 1.00[EUR][1000 genomes] |
rs57751766 | 1.00[EUR][1000 genomes] |
rs58063208 | 1.00[EUR][1000 genomes] |
rs58072732 | 1.00[EUR][1000 genomes] |
rs58194527 | 1.00[EUR][1000 genomes] |
rs58372295 | 1.00[EUR][1000 genomes] |
rs59441074 | 1.00[EUR][1000 genomes] |
rs59834004 | 1.00[EUR][1000 genomes] |
rs60079864 | 1.00[EUR][1000 genomes] |
rs60114889 | 1.00[EUR][1000 genomes] |
rs60304731 | 1.00[EUR][1000 genomes] |
rs61024587 | 1.00[EUR][1000 genomes] |
rs61152857 | 1.00[EUR][1000 genomes] |
rs61518477 | 1.00[EUR][1000 genomes] |
rs7133757 | 1.00[EUR][1000 genomes] |
rs7134836 | 1.00[EUR][1000 genomes] |
rs7299844 | 1.00[EUR][1000 genomes] |
rs7300013 | 1.00[EUR][1000 genomes] |
rs7300654 | 1.00[EUR][1000 genomes] |
rs7303110 | 1.00[EUR][1000 genomes] |
rs7304463 | 1.00[EUR][1000 genomes] |
rs7316657 | 1.00[EUR][1000 genomes] |
rs73270611 | 1.00[EUR][1000 genomes] |
rs73282231 | 1.00[EUR][1000 genomes] |
rs73282241 | 1.00[EUR][1000 genomes] |
rs73282253 | 1.00[EUR][1000 genomes] |
rs73282257 | 1.00[EUR][1000 genomes] |
rs73282264 | 1.00[EUR][1000 genomes] |
rs74077803 | 1.00[EUR][1000 genomes] |
rs74077884 | 1.00[EUR][1000 genomes] |
rs74077888 | 1.00[EUR][1000 genomes] |
rs74078220 | 1.00[EUR][1000 genomes] |
rs74078221 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74078239 | 1.00[EUR][1000 genomes] |
rs74078256 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74078850 | 1.00[EUR][1000 genomes] |
rs74078852 | 1.00[EUR][1000 genomes] |
rs74078861 | 1.00[EUR][1000 genomes] |
rs74079833 | 1.00[EUR][1000 genomes] |
rs74079834 | 1.00[EUR][1000 genomes] |
rs74079835 | 1.00[EUR][1000 genomes] |
rs74079837 | 1.00[EUR][1000 genomes] |
rs74079839 | 1.00[EUR][1000 genomes] |
rs74079840 | 1.00[EUR][1000 genomes] |
rs74079841 | 1.00[EUR][1000 genomes] |
rs74079843 | 1.00[EUR][1000 genomes] |
rs74079844 | 1.00[EUR][1000 genomes] |
rs74079848 | 1.00[EUR][1000 genomes] |
rs74079849 | 1.00[EUR][1000 genomes] |
rs74079850 | 1.00[EUR][1000 genomes] |
rs74079851 | 1.00[EUR][1000 genomes] |
rs74079852 | 1.00[EUR][1000 genomes] |
rs74079853 | 1.00[EUR][1000 genomes] |
rs74079855 | 1.00[EUR][1000 genomes] |
rs74079857 | 1.00[EUR][1000 genomes] |
rs74079859 | 1.00[EUR][1000 genomes] |
rs74079861 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3337301 | chr12:41851654-42093677 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv899040 | chr12:41905897-42181706 | Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv899041 | chr12:42005690-42072514 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv521917 | chr12:42010719-42013167 | Weak transcription | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:42000600-42012000 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |