Variant report
Variant | rs68056864 |
---|---|
Chromosome Location | chr4:142439371-142439372 |
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] |
---|---|
rs10519602 | 0.89[EUR][1000 genomes] |
rs12501765 | 0.87[EUR][1000 genomes] |
rs12506151 | 0.88[EUR][1000 genomes] |
rs12507564 | 0.88[EUR][1000 genomes] |
rs12507887 | 0.88[EUR][1000 genomes] |
rs12508511 | 0.89[EUR][1000 genomes] |
rs12508590 | 0.89[EUR][1000 genomes] |
rs12509285 | 0.82[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs12509822 | 0.87[EUR][1000 genomes] |
rs12510810 | 0.89[EUR][1000 genomes] |
rs12511786 | 0.84[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs12511918 | 0.89[EUR][1000 genomes] |
rs12511983 | 0.89[EUR][1000 genomes] |
rs13105639 | 0.88[EUR][1000 genomes] |
rs13113365 | 0.92[EUR][1000 genomes] |
rs13117984 | 0.92[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs13119177 | 0.91[EUR][1000 genomes] |
rs13129076 | 0.88[EUR][1000 genomes] |
rs13130612 | 0.88[EUR][1000 genomes] |
rs13131082 | 0.88[EUR][1000 genomes] |
rs13133795 | 0.88[EUR][1000 genomes] |
rs13147873 | 0.90[EUR][1000 genomes] |
rs1357158 | 0.92[EUR][1000 genomes] |
rs1402811 | 0.92[EUR][1000 genomes] |
rs1402812 | 0.94[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs1436510 | 0.86[EUR][1000 genomes] |
rs1521760 | 0.86[EUR][1000 genomes] |
rs1521765 | 0.92[AFR][1000 genomes];0.91[EUR][1000 genomes] |
rs1521766 | 0.92[EUR][1000 genomes] |
rs1554477 | 0.88[EUR][1000 genomes] |
rs1581387 | 0.91[EUR][1000 genomes] |
rs1581388 | 0.89[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs1581390 | 0.92[EUR][1000 genomes] |
rs1608019 | 0.91[EUR][1000 genomes] |
rs17007301 | 0.88[EUR][1000 genomes] |
rs17354547 | 0.88[EUR][1000 genomes] |
rs17354568 | 0.88[EUR][1000 genomes] |
rs1949667 | 0.87[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs2090878 | 0.88[EUR][1000 genomes] |
rs2103007 | 0.88[EUR][1000 genomes] |
rs2103008 | 0.87[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs2322181 | 0.88[EUR][1000 genomes] |
rs2322182 | 0.84[ASN][1000 genomes] |
rs34132448 | 0.87[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs34147541 | 0.92[EUR][1000 genomes] |
rs34585213 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs34761999 | 0.91[EUR][1000 genomes] |
rs34963107 | 0.89[EUR][1000 genomes] |
rs35114853 | 0.92[EUR][1000 genomes] |
rs35251884 | 0.81[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs35486128 | 0.91[EUR][1000 genomes] |
rs35815487 | 0.81[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs35881750 | 0.92[EUR][1000 genomes] |
rs35898699 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36043837 | 0.89[EUR][1000 genomes] |
rs4530710 | 0.89[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs4956295 | 0.88[EUR][1000 genomes] |
rs4956297 | 0.90[EUR][1000 genomes] |
rs4956380 | 0.88[EUR][1000 genomes] |
rs4956384 | 0.88[EUR][1000 genomes] |
rs4956389 | 0.89[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs4956396 | 0.92[EUR][1000 genomes] |
rs4956399 | 0.86[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs55726691 | 0.88[EUR][1000 genomes] |
rs55912825 | 0.89[EUR][1000 genomes] |
rs56029027 | 0.89[EUR][1000 genomes] |
rs56051122 | 0.89[EUR][1000 genomes] |
rs56074428 | 0.87[EUR][1000 genomes] |
rs56140725 | 0.87[EUR][1000 genomes] |
rs56155233 | 0.89[EUR][1000 genomes] |
rs60008610 | 0.87[EUR][1000 genomes] |
rs62326572 | 0.90[EUR][1000 genomes] |
rs62326579 | 0.90[EUR][1000 genomes] |
rs62326617 | 0.89[EUR][1000 genomes] |
rs6810477 | 0.87[AFR][1000 genomes];0.91[EUR][1000 genomes] |
rs6812950 | 0.94[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs6816897 | 0.89[EUR][1000 genomes] |
rs6818965 | 0.84[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs6825913 | 0.88[EUR][1000 genomes] |
rs6826356 | 0.94[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs6829748 | 0.87[EUR][1000 genomes] |
rs6831141 | 0.88[EUR][1000 genomes] |
rs6838410 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6842807 | 0.89[EUR][1000 genomes] |
rs6845550 | 0.88[EUR][1000 genomes] |
rs6852094 | 0.84[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs6858423 | 0.89[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs7666040 | 0.86[ASN][1000 genomes] |
rs7666229 | 0.86[ASN][1000 genomes] |
rs7671408 | 0.88[EUR][1000 genomes] |
rs7677830 | 0.89[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs9761396 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv880172 | chr4:142355535-142565089 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv880173 | chr4:142355535-142666106 | Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv830094 | chr4:142411738-142567788 | Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | esv3401979 | chr4:142434442-142803321 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:142435400-142443200 | Weak transcription | Aorta | Aorta |
2 | chr4:142438400-142443200 | Weak transcription | Pancreas | Pancrea |