Variant report
Variant | rs3862877 |
---|---|
Chromosome Location | chr10:45617714-45617715 |
allele | A/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] |
---|---|
rs10751371 | 0.84[EUR][1000 genomes] |
rs10751373 | 0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10793584 | 0.83[EUR][1000 genomes] |
rs12413346 | 0.83[EUR][1000 genomes] |
rs12414221 | 0.83[EUR][1000 genomes] |
rs12415640 | 0.83[EUR][1000 genomes] |
rs1856591 | 0.83[EUR][1000 genomes] |
rs2153333 | 0.86[EUR][1000 genomes] |
rs3862873 | 0.84[EUR][1000 genomes] |
rs3927771 | 0.86[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4068923 | 0.82[EUR][1000 genomes] |
rs4068926 | 0.83[EUR][1000 genomes] |
rs4113135 | 0.87[EUR][1000 genomes] |
rs4379782 | 0.84[EUR][1000 genomes] |
rs4472887 | 0.83[EUR][1000 genomes] |
rs4500437 | 0.82[EUR][1000 genomes] |
rs4511242 | 0.84[EUR][1000 genomes] |
rs4948657 | 0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4948948 | 0.82[EUR][1000 genomes] |
rs4948949 | 0.82[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs6593460 | 0.91[AFR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7080443 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7084047 | 0.87[EUR][1000 genomes] |
rs7902898 | 0.87[EUR][1000 genomes] |
rs7923293 | 0.89[AFR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831848 | chr10:45490176-45667670 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
2 | esv2750897 | chr10:45550145-45820136 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 19 gene(s) | inside rSNPs | diseases |
3 | nsv947903 | chr10:45598715-45657182 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:45617400-45618400 | Weak transcription | Brain Germinal Matrix | brain |