Variant report
Variant | rs1799913 |
---|---|
Chromosome Location | chr11:18047255-18047256 |
allele | A/C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000129158 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10741734 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10766446 | 0.81[EUR][1000 genomes] |
rs10832872 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10832874 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11024446 | 0.89[EUR][1000 genomes] |
rs12292490 | 0.88[EUR][1000 genomes] |
rs1401163 | 0.89[EUR][1000 genomes] |
rs1401164 | 0.89[EUR][1000 genomes] |
rs1518521 | 0.80[EUR][1000 genomes] |
rs1518522 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1607395 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs169806 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1800532 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2041244 | 0.81[EUR][1000 genomes] |
rs2056246 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2071532 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs211106 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs211107 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs211108 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs211140 | 0.80[EUR][1000 genomes] |
rs211141 | 0.80[EUR][1000 genomes] |
rs211144 | 0.80[EUR][1000 genomes] |
rs2237907 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2237908 | 0.94[EUR][1000 genomes] |
rs2237909 | 0.81[EUR][1000 genomes] |
rs2237911 | 0.80[EUR][1000 genomes] |
rs2283233 | 0.81[EUR][1000 genomes] |
rs2283235 | 0.81[EUR][1000 genomes] |
rs2299625 | 0.89[EUR][1000 genomes] |
rs508924 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs517005 | 0.89[EUR][1000 genomes] |
rs544437 | 0.88[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs546383 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs572940 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs593839 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs652458 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs654734 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs684302 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs685249 | 0.85[AMR][1000 genomes] |
rs685657 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs72862028 | 0.88[EUR][1000 genomes] |
rs7927135 | 0.81[EUR][1000 genomes] |
rs7933505 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs887242 | 0.88[EUR][1000 genomes] |
rs9787863 | 0.81[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949248 | chr11:17791822-18692687 | Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 156 gene(s) | inside rSNPs | diseases |
2 | nsv897026 | chr11:17823296-18084878 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv832079 | chr11:17927967-18047743 | Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:18035600-18048600 | Weak transcription | Ovary | ovary |
2 | chr11:18042600-18064600 | Weak transcription | Aorta | Aorta |