Variant report
Variant | rs73091012 |
---|---|
Chromosome Location | chr3:56091781-56091782 |
allele | A/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] |
---|---|
rs10461036 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10510779 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10510780 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10510781 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11428238 | 0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs13315826 | 0.92[EUR][1000 genomes] |
rs13326476 | 0.92[EUR][1000 genomes] |
rs13326628 | 0.92[EUR][1000 genomes] |
rs17056469 | 0.90[EUR][1000 genomes] |
rs17056472 | 0.89[EUR][1000 genomes] |
rs17216545 | 0.93[ASN][1000 genomes] |
rs17235263 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs17235291 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs17235305 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs17235368 | 0.92[EUR][1000 genomes] |
rs17235375 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs17235382 | 0.92[EUR][1000 genomes] |
rs17235389 | 0.92[EUR][1000 genomes] |
rs17235396 | 0.92[EUR][1000 genomes] |
rs17825159 | 0.89[EUR][1000 genomes] |
rs17825183 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs17825189 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs17825201 | 0.92[EUR][1000 genomes] |
rs17825207 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17825213 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17825219 | 0.92[EUR][1000 genomes] |
rs17825278 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1982766 | 0.89[EUR][1000 genomes] |
rs28463735 | 0.89[EUR][1000 genomes] |
rs28464790 | 0.92[EUR][1000 genomes] |
rs35563958 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs56101867 | 0.89[EUR][1000 genomes] |
rs58375176 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs61401343 | 0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6800841 | 0.87[EUR][1000 genomes] |
rs6805331 | 0.85[EUR][1000 genomes] |
rs6807938 | 0.87[EUR][1000 genomes] |
rs73089182 | 0.84[EUR][1000 genomes] |
rs73089299 | 0.92[EUR][1000 genomes] |
rs73091008 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs73091011 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091052 | 0.89[EUR][1000 genomes] |
rs73091061 | 0.89[EUR][1000 genomes] |
rs73091207 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs73091213 | 0.91[EUR][1000 genomes] |
rs73091231 | 0.92[EUR][1000 genomes] |
rs73091236 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs73091241 | 0.93[EUR][1000 genomes] |
rs73091242 | 0.89[EUR][1000 genomes] |
rs7625220 | 0.88[EUR][1000 genomes] |
rs7625230 | 0.87[EUR][1000 genomes] |
rs7625422 | 0.86[EUR][1000 genomes] |
rs7629639 | 0.93[EUR][1000 genomes] |
rs7629769 | 0.89[EUR][1000 genomes] |
rs7632887 | 0.88[EUR][1000 genomes] |
rs7632901 | 0.88[EUR][1000 genomes] |
rs7651932 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs923127 | 0.89[EUR][1000 genomes] |
rs923128 | 0.89[EUR][1000 genomes] |
rs9311594 | 0.91[EUR][1000 genomes] |
rs9311595 | 0.92[EUR][1000 genomes] |
rs9311596 | 0.90[EUR][1000 genomes] |
rs9810107 | 0.92[EUR][1000 genomes] |
rs9810354 | 0.88[EUR][1000 genomes] |
rs9811060 | 0.92[EUR][1000 genomes] |
rs9811789 | 0.92[EUR][1000 genomes] |
rs9811790 | 0.92[EUR][1000 genomes] |
rs9814900 | 0.92[EUR][1000 genomes] |
rs9815611 | 0.92[EUR][1000 genomes] |
rs9817131 | 0.89[EUR][1000 genomes] |
rs9817492 | 0.92[EUR][1000 genomes] |
rs9817542 | 0.92[EUR][1000 genomes] |
rs9819890 | 0.87[EUR][1000 genomes] |
rs9820348 | 0.84[EUR][1000 genomes] |
rs9820493 | 0.89[EUR][1000 genomes] |
rs9827514 | 0.92[EUR][1000 genomes] |
rs9828337 | 0.92[EUR][1000 genomes] |
rs9830503 | 0.89[EUR][1000 genomes] |
rs9831925 | 0.90[EUR][1000 genomes] |
rs9837290 | 0.92[EUR][1000 genomes] |
rs9838245 | 0.89[EUR][1000 genomes] |
rs9842617 | 0.87[EUR][1000 genomes] |
rs9844291 | 0.92[EUR][1000 genomes] |
rs9854960 | 0.89[EUR][1000 genomes] |
rs9855148 | 0.92[EUR][1000 genomes] |
rs9855836 | 0.92[EUR][1000 genomes] |
rs9857687 | 0.87[EUR][1000 genomes] |
rs9860909 | 0.92[EUR][1000 genomes] |
rs9861486 | 0.92[EUR][1000 genomes] |
rs9862215 | 0.92[EUR][1000 genomes] |
rs9865648 | 0.89[EUR][1000 genomes] |
rs9865958 | 0.89[EUR][1000 genomes] |
rs9866234 | 0.89[EUR][1000 genomes] |
rs9866951 | 0.92[EUR][1000 genomes] |
rs9869654 | 0.92[EUR][1000 genomes] |
rs9870248 | 0.90[EUR][1000 genomes] |
rs9870989 | 0.92[EUR][1000 genomes] |
rs9871223 | 0.92[EUR][1000 genomes] |
rs9874507 | 0.91[EUR][1000 genomes] |
rs9874662 | 0.89[EUR][1000 genomes] |
rs9880824 | 0.92[EUR][1000 genomes] |
rs9881126 | 0.92[EUR][1000 genomes] |
rs9881968 | 0.89[EUR][1000 genomes] |
rs9882373 | 0.92[EUR][1000 genomes] |
rs9883636 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1013063 | chr3:55835413-56173713 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1009709 | chr3:56000827-56294945 | Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:56090200-56094000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |