Variant report
Variant | rs60010024 |
---|---|
Chromosome Location | chr18:12181774-12181775 |
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] |
---|---|
rs10445425 | 0.85[EUR][1000 genomes] |
rs10445426 | 0.85[EUR][1000 genomes] |
rs11080549 | 0.87[EUR][1000 genomes] |
rs11080550 | 0.81[EUR][1000 genomes] |
rs11877166 | 0.89[EUR][1000 genomes] |
rs12454161 | 0.82[EUR][1000 genomes] |
rs12604417 | 0.86[EUR][1000 genomes] |
rs12605170 | 0.82[EUR][1000 genomes] |
rs12605187 | 0.83[EUR][1000 genomes] |
rs12605231 | 0.80[EUR][1000 genomes] |
rs12607481 | 0.85[EUR][1000 genomes] |
rs12955316 | 0.87[EUR][1000 genomes] |
rs12963518 | 0.91[EUR][1000 genomes] |
rs12965571 | 0.86[EUR][1000 genomes] |
rs12969917 | 0.84[EUR][1000 genomes] |
rs1986750 | 0.84[EUR][1000 genomes] |
rs1986751 | 0.84[EUR][1000 genomes] |
rs2276370 | 0.86[EUR][1000 genomes] |
rs2851905 | 0.86[EUR][1000 genomes] |
rs2851907 | 0.83[EUR][1000 genomes] |
rs2851923 | 0.87[EUR][1000 genomes] |
rs28592744 | 0.87[EUR][1000 genomes] |
rs28648884 | 0.88[EUR][1000 genomes] |
rs34036584 | 0.93[EUR][1000 genomes] |
rs34185303 | 0.85[EUR][1000 genomes] |
rs4239305 | 0.88[EUR][1000 genomes] |
rs4261610 | 0.87[EUR][1000 genomes] |
rs4296321 | 0.91[EUR][1000 genomes] |
rs4299212 | 0.91[EUR][1000 genomes] |
rs4303617 | 0.91[EUR][1000 genomes] |
rs4306582 | 0.91[EUR][1000 genomes] |
rs4327115 | 0.90[EUR][1000 genomes] |
rs4337367 | 0.91[EUR][1000 genomes] |
rs4347689 | 0.82[EUR][1000 genomes] |
rs4402627 | 0.91[EUR][1000 genomes] |
rs4416083 | 0.87[EUR][1000 genomes] |
rs4417605 | 0.85[EUR][1000 genomes] |
rs4417606 | 0.85[EUR][1000 genomes] |
rs4419117 | 0.84[EUR][1000 genomes] |
rs4456573 | 0.91[EUR][1000 genomes] |
rs4462671 | 0.87[EUR][1000 genomes] |
rs4464145 | 0.91[EUR][1000 genomes] |
rs4480870 | 0.91[EUR][1000 genomes] |
rs4519391 | 0.87[EUR][1000 genomes] |
rs4528645 | 0.83[EUR][1000 genomes] |
rs4528648 | 0.86[EUR][1000 genomes] |
rs4538071 | 0.88[EUR][1000 genomes] |
rs4569357 | 0.86[EUR][1000 genomes] |
rs4572475 | 0.91[EUR][1000 genomes] |
rs4583319 | 0.83[EUR][1000 genomes] |
rs4591211 | 0.81[EUR][1000 genomes] |
rs4621045 | 0.87[EUR][1000 genomes] |
rs4796945 | 0.84[EUR][1000 genomes] |
rs4796946 | 0.86[EUR][1000 genomes] |
rs4796947 | 0.86[EUR][1000 genomes] |
rs4797623 | 0.84[EUR][1000 genomes] |
rs4797624 | 0.88[EUR][1000 genomes] |
rs4797625 | 0.87[EUR][1000 genomes] |
rs4797631 | 0.91[EUR][1000 genomes] |
rs4797632 | 0.91[EUR][1000 genomes] |
rs4797633 | 0.91[EUR][1000 genomes] |
rs4797634 | 0.91[EUR][1000 genomes] |
rs4797636 | 0.91[EUR][1000 genomes] |
rs4797637 | 0.91[EUR][1000 genomes] |
rs4797640 | 0.85[EUR][1000 genomes] |
rs55979571 | 0.82[EUR][1000 genomes] |
rs56101236 | 0.86[EUR][1000 genomes] |
rs57801464 | 0.85[EUR][1000 genomes] |
rs60401418 | 0.86[EUR][1000 genomes] |
rs61343100 | 0.89[EUR][1000 genomes] |
rs61606757 | 0.81[EUR][1000 genomes] |
rs62097608 | 0.90[EUR][1000 genomes] |
rs62097613 | 0.95[EUR][1000 genomes] |
rs62099061 | 0.85[EUR][1000 genomes] |
rs62099085 | 0.80[EUR][1000 genomes] |
rs6505715 | 0.84[EUR][1000 genomes] |
rs6505717 | 0.87[EUR][1000 genomes] |
rs6505720 | 0.89[EUR][1000 genomes] |
rs6505725 | 0.92[EUR][1000 genomes] |
rs7226400 | 0.87[EUR][1000 genomes] |
rs7227857 | 0.90[EUR][1000 genomes] |
rs7239346 | 0.88[EUR][1000 genomes] |
rs7239448 | 0.85[EUR][1000 genomes] |
rs7239947 | 0.91[EUR][1000 genomes] |
rs7240093 | 0.88[EUR][1000 genomes] |
rs7242541 | 0.86[EUR][1000 genomes] |
rs7243248 | 0.88[EUR][1000 genomes] |
rs7244723 | 0.87[EUR][1000 genomes] |
rs73410960 | 0.91[EUR][1000 genomes] |
rs8082868 | 0.90[EUR][1000 genomes] |
rs8082888 | 0.89[EUR][1000 genomes] |
rs8087637 | 0.91[EUR][1000 genomes] |
rs8091463 | 0.87[EUR][1000 genomes] |
rs8091585 | 0.87[EUR][1000 genomes] |
rs8093417 | 0.86[EUR][1000 genomes] |
rs8095234 | 0.86[EUR][1000 genomes] |
rs8095647 | 0.86[EUR][1000 genomes] |
rs8099792 | 0.81[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs9303759 | 0.88[EUR][1000 genomes] |
rs9303760 | 0.86[EUR][1000 genomes] |
rs9945491 | 0.84[EUR][1000 genomes] |
rs9948384 | 0.86[EUR][1000 genomes] |
rs9949350 | 0.84[EUR][1000 genomes] |
rs9951744 | 0.84[EUR][1000 genomes] |
rs9951822 | 0.84[EUR][1000 genomes] |
rs9951904 | 0.87[EUR][1000 genomes] |
rs9951929 | 0.84[EUR][1000 genomes] |
rs9953892 | 0.83[EUR][1000 genomes] |
rs9954852 | 0.85[EUR][1000 genomes] |
rs9954861 | 0.89[EUR][1000 genomes] |
rs9954884 | 0.89[EUR][1000 genomes] |
rs9955629 | 0.91[EUR][1000 genomes] |
rs9956465 | 0.87[EUR][1000 genomes] |
rs9956997 | 0.87[EUR][1000 genomes] |
rs9957303 | 0.87[EUR][1000 genomes] |
rs9959641 | 0.87[EUR][1000 genomes] |
rs9963587 | 0.86[EUR][1000 genomes] |
rs9965004 | 0.86[EUR][1000 genomes] |
rs9965108 | 0.88[EUR][1000 genomes] |
rs9966965 | 0.83[EUR][1000 genomes] |
rs9967372 | 0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1063125 | chr18:12046892-12918251 | Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 130 gene(s) | inside rSNPs | diseases |
2 | nsv1055343 | chr18:12107012-12226356 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv491873 | chr18:12159445-12739784 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 79 gene(s) | inside rSNPs | diseases |
4 | nsv960252 | chr18:12161216-12220798 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:12154200-12183800 | Weak transcription | Pancreas | Pancrea |