Variant report
Variant | rs2035056 |
---|---|
Chromosome Location | chr4:87139379-87139380 |
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] |
---|---|
rs10003556 | 0.90[ASN][1000 genomes] |
rs10003756 | 0.81[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10004539 | 0.93[ASN][1000 genomes] |
rs10009161 | 0.90[ASN][1000 genomes] |
rs10010011 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10016847 | 0.90[ASN][1000 genomes] |
rs10019871 | 0.90[ASN][1000 genomes] |
rs10022904 | 0.98[ASN][1000 genomes] |
rs10026060 | 0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10026338 | 0.81[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10029339 | 0.94[ASN][1000 genomes] |
rs10034428 | 0.90[ASN][1000 genomes] |
rs10213302 | 0.93[ASN][1000 genomes] |
rs10213451 | 0.93[ASN][1000 genomes] |
rs10213453 | 0.93[ASN][1000 genomes] |
rs10516769 | 0.98[ASN][1000 genomes] |
rs1108429 | 0.84[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11097101 | 0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11097102 | 0.90[ASN][1000 genomes] |
rs11097103 | 0.90[ASN][1000 genomes] |
rs11935211 | 0.94[ASN][1000 genomes] |
rs12500319 | 0.86[ASN][1000 genomes] |
rs12640392 | 0.82[ASN][1000 genomes] |
rs12646076 | 0.90[ASN][1000 genomes] |
rs12650052 | 0.81[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1460750 | 0.90[ASN][1000 genomes] |
rs1460758 | 0.94[ASN][1000 genomes] |
rs1460759 | 0.94[ASN][1000 genomes] |
rs1460760 | 0.90[ASN][1000 genomes] |
rs1460761 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1460763 | 0.90[ASN][1000 genomes] |
rs1460764 | 0.90[ASN][1000 genomes] |
rs1599313 | 0.90[ASN][1000 genomes] |
rs1599314 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17011421 | 0.90[ASN][1000 genomes] |
rs17011460 | 0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17011540 | 0.93[ASN][1000 genomes] |
rs17011547 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17011564 | 0.90[ASN][1000 genomes] |
rs17011584 | 0.95[ASN][1000 genomes] |
rs17011588 | 0.84[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs17011592 | 0.98[ASN][1000 genomes] |
rs17011654 | 0.87[ASN][1000 genomes] |
rs17011655 | 0.82[ASN][1000 genomes] |
rs1903360 | 0.90[ASN][1000 genomes] |
rs1903361 | 0.93[ASN][1000 genomes] |
rs2035057 | 0.94[ASN][1000 genomes] |
rs2035058 | 0.87[ASN][1000 genomes] |
rs2199308 | 0.90[ASN][1000 genomes] |
rs2199309 | 0.90[ASN][1000 genomes] |
rs28425193 | 0.98[ASN][1000 genomes] |
rs28583812 | 0.98[ASN][1000 genomes] |
rs28642002 | 0.93[ASN][1000 genomes] |
rs2869421 | 0.90[ASN][1000 genomes] |
rs2869422 | 0.98[ASN][1000 genomes] |
rs28722990 | 0.98[ASN][1000 genomes] |
rs28791572 | 0.93[ASN][1000 genomes] |
rs28803851 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs28812808 | 0.94[ASN][1000 genomes] |
rs28830922 | 0.91[ASN][1000 genomes] |
rs28839895 | 0.93[ASN][1000 genomes] |
rs28870188 | 0.89[ASN][1000 genomes] |
rs28896887 | 0.93[ASN][1000 genomes] |
rs2904090 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4114893 | 0.80[ASN][1000 genomes] |
rs4132490 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4561895 | 0.93[ASN][1000 genomes] |
rs59124829 | 0.93[ASN][1000 genomes] |
rs6531905 | 0.90[ASN][1000 genomes] |
rs6531906 | 0.94[ASN][1000 genomes] |
rs6531907 | 0.94[ASN][1000 genomes] |
rs6531909 | 0.94[ASN][1000 genomes] |
rs6531910 | 0.94[ASN][1000 genomes] |
rs6531911 | 0.94[ASN][1000 genomes] |
rs67768527 | 0.84[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6814005 | 0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6817452 | 0.90[ASN][1000 genomes] |
rs6821819 | 0.90[ASN][1000 genomes] |
rs6825521 | 0.90[ASN][1000 genomes] |
rs6826951 | 0.90[ASN][1000 genomes] |
rs6827405 | 0.87[ASN][1000 genomes] |
rs6827698 | 0.90[ASN][1000 genomes] |
rs6828947 | 0.90[ASN][1000 genomes] |
rs6829870 | 0.90[ASN][1000 genomes] |
rs6832259 | 0.94[ASN][1000 genomes] |
rs6844363 | 0.84[ASN][1000 genomes] |
rs6844365 | 0.90[ASN][1000 genomes] |
rs6845605 | 0.90[ASN][1000 genomes] |
rs6845742 | 0.90[ASN][1000 genomes] |
rs7440491 | 0.90[ASN][1000 genomes] |
rs7655797 | 0.90[ASN][1000 genomes] |
rs7657056 | 0.90[ASN][1000 genomes] |
rs7663388 | 0.93[ASN][1000 genomes] |
rs7663763 | 0.93[ASN][1000 genomes] |
rs7668374 | 0.84[ASN][1000 genomes] |
rs7669487 | 0.90[ASN][1000 genomes] |
rs7678480 | 0.93[ASN][1000 genomes] |
rs7680934 | 0.94[ASN][1000 genomes] |
rs7685419 | 0.84[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7685683 | 0.93[ASN][1000 genomes] |
rs7687771 | 0.90[ASN][1000 genomes] |
rs7695707 | 0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7699047 | 0.90[ASN][1000 genomes] |
rs9307016 | 0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9654155 | 0.89[ASN][1000 genomes] |
rs9884127 | 0.94[ASN][1000 genomes] |
rs9994303 | 0.82[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9996693 | 0.90[ASN][1000 genomes] |
rs9997633 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9999403 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1003585 | chr4:86957967-87250436 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv879521 | chr4:86979927-87165758 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv594786 | chr4:87076360-87609320 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:87132800-87139800 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
2 | chr4:87136400-87140000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
3 | chr4:87136800-87140000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
4 | chr4:87138800-87139400 | Weak transcription | A549 | lung |
5 | chr4:87138800-87140000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
6 | chr4:87138800-87140200 | Weak transcription | NHDF-Ad | bronchial |