Variant report
Variant | rs6551350 |
---|---|
Chromosome Location | chr3:88623347-88623348 |
allele | C/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] |
---|---|
rs10511138 | 0.88[ASN][1000 genomes] |
rs11128053 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12486895 | 0.99[ASN][1000 genomes] |
rs12487385 | 0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12487560 | 0.89[ASN][1000 genomes] |
rs12487623 | 0.89[ASN][1000 genomes] |
rs12488032 | 0.99[ASN][1000 genomes] |
rs12488286 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12488396 | 1.00[ASN][1000 genomes] |
rs12489078 | 0.84[ASN][1000 genomes] |
rs12490357 | 0.89[ASN][1000 genomes] |
rs12491633 | 0.86[ASN][1000 genomes] |
rs12491766 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12494001 | 0.87[ASN][1000 genomes] |
rs12495478 | 0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12495558 | 0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12629360 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12637931 | 0.89[ASN][1000 genomes] |
rs12639499 | 0.85[ASN][1000 genomes] |
rs13073581 | 0.85[ASN][1000 genomes] |
rs13321865 | 0.81[ASN][1000 genomes] |
rs17559821 | 0.85[ASN][1000 genomes] |
rs17560386 | 0.89[ASN][1000 genomes] |
rs1979751 | 0.88[ASN][1000 genomes] |
rs2132362 | 0.84[ASN][1000 genomes] |
rs28447483 | 0.89[ASN][1000 genomes] |
rs28784899 | 0.88[ASN][1000 genomes] |
rs28876760 | 0.89[ASN][1000 genomes] |
rs55694746 | 0.99[ASN][1000 genomes] |
rs56076642 | 0.89[ASN][1000 genomes] |
rs56076980 | 0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs56359806 | 0.88[ASN][1000 genomes] |
rs59752267 | 1.00[ASN][1000 genomes] |
rs59757044 | 0.85[ASN][1000 genomes] |
rs60418303 | 1.00[ASN][1000 genomes] |
rs60574566 | 1.00[ASN][1000 genomes] |
rs61176217 | 1.00[ASN][1000 genomes] |
rs67260046 | 0.85[ASN][1000 genomes] |
rs6776183 | 0.86[ASN][1000 genomes] |
rs6778723 | 0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6794212 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6799848 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6802531 | 0.82[ASN][1000 genomes] |
rs6803194 | 0.88[AFR][1000 genomes] |
rs73134314 | 0.88[ASN][1000 genomes] |
rs73134400 | 0.86[ASN][1000 genomes] |
rs73136414 | 0.84[ASN][1000 genomes] |
rs73136419 | 0.84[ASN][1000 genomes] |
rs73146499 | 0.99[ASN][1000 genomes] |
rs73152336 | 0.89[ASN][1000 genomes] |
rs7430981 | 0.88[ASN][1000 genomes] |
rs7431370 | 0.83[ASN][1000 genomes] |
rs7432988 | 1.00[ASN][1000 genomes] |
rs7433029 | 1.00[ASN][1000 genomes] |
rs7637716 | 0.86[ASN][1000 genomes] |
rs7652836 | 0.89[ASN][1000 genomes] |
rs9824652 | 0.82[ASN][1000 genomes] |
rs9856843 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916330 | chr3:88083580-88884125 | Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv3906 | chr3:88609226-88654550 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:88622200-88623400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr3:88622400-88627800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
3 | chr3:88622800-88623600 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
4 | chr3:88623200-88624000 | Enhancers | Pancreatic Islets | Pancreatic Islet |