Variant report
Variant | rs2052511 |
---|---|
Chromosome Location | chr5:164618886-164618887 |
allele | C/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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10076942 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11743682 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11750392 | 0.92[ASN][1000 genomes] |
rs13164844 | 1.00[ASN][1000 genomes] |
rs13175931 | 1.00[ASN][1000 genomes] |
rs1368423 | 0.88[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1473186 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17332900 | 0.92[ASN][1000 genomes] |
rs2112641 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs253536 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2861088 | 0.88[EUR][1000 genomes] |
rs2861089 | 0.88[EUR][1000 genomes] |
rs2861093 | 0.83[EUR][1000 genomes] |
rs34809058 | 1.00[ASN][1000 genomes] |
rs35322903 | 1.00[ASN][1000 genomes] |
rs35839763 | 1.00[ASN][1000 genomes] |
rs36070089 | 0.92[ASN][1000 genomes] |
rs36113677 | 1.00[ASN][1000 genomes] |
rs4283809 | 0.89[EUR][1000 genomes] |
rs4552632 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4563646 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6869965 | 0.83[EUR][1000 genomes] |
rs6884321 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7444721 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7447465 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs766120 | 0.87[EUR][1000 genomes] |
rs766122 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs9314053 | 0.89[EUR][1000 genomes] |
rs982305 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv995060 | chr5:163660200-164620500 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv528624 | chr5:164319435-164701201 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1033866 | chr5:164419608-164677758 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1027138 | chr5:164563093-164852655 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv537937 | chr5:164563093-164852655 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1028006 | chr5:164563293-164852516 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv537938 | chr5:164563293-164852516 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv1027103 | chr5:164606534-164694498 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:164618000-164619800 | Weak transcription | Primary monocytes fromperipheralblood | blood |
2 | chr5:164618000-164619800 | Weak transcription | Monocytes-CD14+_RO01746 | blood |