Variant report
Variant | rs1544022 |
---|---|
Chromosome Location | chr3:109330640-109330641 |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11708820 | 0.84[EUR][1000 genomes] |
rs11716678 | 0.85[EUR][1000 genomes] |
rs12485442 | 0.85[EUR][1000 genomes] |
rs1528901 | 0.81[EUR][1000 genomes] |
rs1528906 | 0.85[EUR][1000 genomes] |
rs1534634 | 0.85[EUR][1000 genomes] |
rs1609370 | 0.81[EUR][1000 genomes] |
rs1609371 | 0.81[EUR][1000 genomes] |
rs1612794 | 0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs16855902 | 0.84[EUR][1000 genomes] |
rs1729603 | 0.81[EUR][1000 genomes] |
rs1729608 | 0.81[EUR][1000 genomes] |
rs1729610 | 0.81[EUR][1000 genomes] |
rs1732173 | 0.81[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs1732191 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1732206 | 0.85[EUR][1000 genomes] |
rs17656128 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs1919468 | 0.84[EUR][1000 genomes] |
rs1950051 | 0.84[EUR][1000 genomes] |
rs1950053 | 0.84[EUR][1000 genomes] |
rs2222787 | 0.85[EUR][1000 genomes] |
rs6775168 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs72491106 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7653616 | 0.84[EUR][1000 genomes] |
rs950690 | 0.80[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv460814 | chr3:109195046-109381428 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv591268 | chr3:109195046-109381428 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv470827 | chr3:109195046-109433855 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:109327400-109331600 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr3:109330400-109331000 | Enhancers | Dnd41 | blood |