Variant report
Variant | rs34460044 |
---|---|
Chromosome Location | chr1:222580204-222580205 |
allele | A/G |
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] |
---|---|
rs11485175 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11581653 | 0.91[EUR][1000 genomes] |
rs11589561 | 0.91[EUR][1000 genomes] |
rs11591051 | 0.91[EUR][1000 genomes] |
rs1386580 | 0.91[EUR][1000 genomes] |
rs17163094 | 0.94[ASN][1000 genomes] |
rs17163107 | 0.93[ASN][1000 genomes] |
rs17461834 | 0.90[EUR][1000 genomes] |
rs17462264 | 0.91[EUR][1000 genomes] |
rs17508365 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1906271 | 0.90[EUR][1000 genomes] |
rs1906272 | 0.93[ASN][1000 genomes] |
rs1906273 | 0.91[EUR][1000 genomes] |
rs34930055 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35052617 | 0.91[EUR][1000 genomes] |
rs35061493 | 0.88[EUR][1000 genomes] |
rs35077442 | 0.91[EUR][1000 genomes] |
rs35763770 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35844598 | 0.91[EUR][1000 genomes] |
rs4436398 | 0.91[EUR][1000 genomes] |
rs4846366 | 0.93[ASN][1000 genomes] |
rs4846749 | 0.91[ASN][1000 genomes] |
rs73119096 | 0.93[ASN][1000 genomes] |
rs765233 | 0.90[EUR][1000 genomes] |
rs765308 | 0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv873203 | chr1:222332906-222775000 | Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv873204 | chr1:222484745-222611210 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv999185 | chr1:222500725-223278032 | Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 45 gene(s) | inside rSNPs | diseases |
4 | nsv535304 | chr1:222500725-223278032 | Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 45 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:222578800-222581000 | Weak transcription | Primary T helper cells fromperipheralblood | blood |