Variant report
Variant | rs11031787 |
---|---|
Chromosome Location | chr11:32462206-32462207 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:32460248..32463699-chr11:32486018..32490383,4 | K562 | blood: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-EIF3M-2 | chr11:32459391-32462950 | ENSG00000183242 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10835913 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10835914 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10835915 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10835921 | 0.89[EUR][1000 genomes] |
rs11031778 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11031788 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11031790 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12222697 | 0.91[EUR][1000 genomes] |
rs12224136 | 0.91[EUR][1000 genomes] |
rs12575247 | 0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs1799925 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2234585 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs2418912 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2900753 | 0.96[EUR][1000 genomes] |
rs34163689 | 0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3858449 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs3858451 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs5030141 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs5030171 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs59518979 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61889251 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs61889255 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs61889256 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs61891673 | 0.91[EUR][1000 genomes] |
rs61891675 | 0.83[EUR][1000 genomes] |
rs61891678 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832108 | chr11:32395937-32560583 | Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | nsv1044547 | chr11:32435753-32465233 | Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | esv2753303 | chr11:32447324-32494924 | Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv1051559 | chr11:32447347-32465233 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:32457000-32462600 | Bivalent/Poised TSS | Fetal Kidney | kidney |
2 | chr11:32461000-32463200 | Bivalent Enhancer | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
3 | chr11:32461400-32462600 | Weak transcription | Dnd41 | blood |