Variant report
Variant | rs380262 |
---|---|
Chromosome Location | chr3:21416219-21416220 |
allele | A/C |
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] |
---|---|
rs148456 | 0.81[EUR][1000 genomes] |
rs1507814 | 0.81[EUR][1000 genomes] |
rs1621650 | 0.81[EUR][1000 genomes] |
rs1656662 | 0.81[EUR][1000 genomes] |
rs1656666 | 0.81[EUR][1000 genomes] |
rs1697707 | 0.86[AFR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1697711 | 0.81[EUR][1000 genomes] |
rs1697713 | 0.81[EUR][1000 genomes] |
rs1702772 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs341856 | 0.81[CEU][hapmap];0.86[TSI][hapmap];0.80[EUR][1000 genomes] |
rs341863 | 0.81[EUR][1000 genomes] |
rs378681 | 0.84[AFR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs386201 | 0.83[AFR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs388126 | 0.81[EUR][1000 genomes] |
rs397440 | 0.81[EUR][1000 genomes] |
rs400572 | 0.81[EUR][1000 genomes] |
rs405338 | 0.81[EUR][1000 genomes] |
rs407886 | 0.81[EUR][1000 genomes] |
rs411616 | 0.85[CEU][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes] |
rs421433 | 0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs423727 | 0.81[EUR][1000 genomes] |
rs423879 | 0.85[CEU][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes] |
rs430203 | 0.81[EUR][1000 genomes] |
rs442920 | 0.80[CEU][hapmap] |
rs446992 | 0.81[EUR][1000 genomes] |
rs449166 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs449973 | 0.80[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs776642 | 0.84[CEU][hapmap] |
rs9820551 | 0.86[AFR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs9866352 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834630 | chr3:21311619-21491327 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1011516 | chr3:21337788-21472093 | Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv876609 | chr3:21337956-21424985 | Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv876610 | chr3:21345639-21424985 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1006471 | chr3:21385627-21596955 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv534005 | chr3:21387588-22003293 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
7 | nsv1000828 | chr3:21399870-21565580 | Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv536515 | chr3:21399870-21565580 | Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:21414600-21418200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr3:21414800-21418000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |