Variant report
Variant | rs1833892 |
---|---|
Chromosome Location | chr5:40884634-40884635 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:40839617..40842545-chr5:40884343..40886931,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000132357 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10064232 | 1.00[ASN][1000 genomes] |
rs1070445 | 0.94[ASN][1000 genomes] |
rs1097592 | 0.94[ASN][1000 genomes] |
rs1097604 | 0.94[ASN][1000 genomes] |
rs1530811 | 1.00[ASN][1000 genomes] |
rs154273 | 0.88[ASN][1000 genomes] |
rs154274 | 0.94[ASN][1000 genomes] |
rs1631661 | 0.88[ASN][1000 genomes] |
rs1697929 | 0.94[ASN][1000 genomes] |
rs1697937 | 0.94[ASN][1000 genomes] |
rs184436 | 0.94[ASN][1000 genomes] |
rs187274 | 0.88[ASN][1000 genomes] |
rs192962 | 0.94[ASN][1000 genomes] |
rs2262009 | 0.94[ASN][1000 genomes] |
rs249443 | 0.88[ASN][1000 genomes] |
rs249444 | 0.88[ASN][1000 genomes] |
rs29762 | 0.88[ASN][1000 genomes] |
rs29763 | 0.88[ASN][1000 genomes] |
rs29764 | 0.88[ASN][1000 genomes] |
rs323554 | 1.00[ASN][1000 genomes] |
rs323556 | 0.94[ASN][1000 genomes] |
rs323560 | 0.94[ASN][1000 genomes] |
rs323562 | 0.94[ASN][1000 genomes] |
rs39794 | 0.88[ASN][1000 genomes] |
rs408238 | 1.00[ASN][1000 genomes] |
rs418494 | 0.94[ASN][1000 genomes] |
rs42515 | 0.88[ASN][1000 genomes] |
rs433730 | 0.94[ASN][1000 genomes] |
rs442869 | 0.88[ASN][1000 genomes] |
rs466960 | 0.88[ASN][1000 genomes] |
rs694217 | 1.00[ASN][1000 genomes] |
rs7717507 | 1.00[ASN][1000 genomes] |
rs837378 | 0.94[ASN][1000 genomes] |
rs837381 | 0.94[ASN][1000 genomes] |
rs837382 | 0.94[ASN][1000 genomes] |
rs837384 | 0.94[ASN][1000 genomes] |
rs837385 | 0.94[ASN][1000 genomes] |
rs837389 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv880438 | chr5:40753877-40900717 | Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 160 gene(s) | inside rSNPs | diseases |
2 | esv3444044 | chr5:40860244-40888483 | Enhancers ZNF genes & repeats Weak transcription Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv881467 | chr5:40869802-41008650 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | esv2757114 | chr5:40874078-41009282 | Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | esv2759341 | chr5:40874078-41009282 | Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
6 | nsv823055 | chr5:40875708-41004839 | Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
7 | esv35077 | chr5:40875843-41000671 | Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:40882400-40884800 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr5:40883600-40885200 | Active TSS | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |