Variant report
Variant | rs9863971 |
---|---|
Chromosome Location | chr3:89257627-89257628 |
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] |
---|---|
rs13316356 | 0.89[ASN][1000 genomes] |
rs13323078 | 0.80[ASN][1000 genomes] |
rs1398531 | 0.96[ASN][1000 genomes] |
rs1567731 | 0.87[ASN][1000 genomes] |
rs17026816 | 0.89[ASN][1000 genomes] |
rs17738248 | 0.91[ASN][1000 genomes] |
rs17800347 | 0.82[ASN][1000 genomes] |
rs17800551 | 0.87[ASN][1000 genomes] |
rs2063590 | 0.87[ASN][1000 genomes] |
rs2137487 | 0.87[ASN][1000 genomes] |
rs2137488 | 0.87[ASN][1000 genomes] |
rs28620812 | 0.87[ASN][1000 genomes] |
rs28834186 | 0.91[ASN][1000 genomes] |
rs4857497 | 0.91[ASN][1000 genomes] |
rs4857502 | 0.87[ASN][1000 genomes] |
rs57468276 | 0.94[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62274619 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs62274634 | 0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs62274635 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62274654 | 0.99[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62274656 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62274657 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62274981 | 0.89[ASN][1000 genomes] |
rs62274982 | 0.89[ASN][1000 genomes] |
rs62274984 | 0.85[ASN][1000 genomes] |
rs62274986 | 0.87[ASN][1000 genomes] |
rs62278161 | 0.96[ASN][1000 genomes] |
rs62278163 | 0.96[ASN][1000 genomes] |
rs62278164 | 0.91[ASN][1000 genomes] |
rs62278166 | 0.91[ASN][1000 genomes] |
rs62278168 | 0.91[ASN][1000 genomes] |
rs62278170 | 0.91[ASN][1000 genomes] |
rs62278171 | 0.91[ASN][1000 genomes] |
rs62278172 | 0.91[ASN][1000 genomes] |
rs6773815 | 0.91[ASN][1000 genomes] |
rs6776281 | 0.96[ASN][1000 genomes] |
rs6786204 | 0.91[ASN][1000 genomes] |
rs6786328 | 0.91[ASN][1000 genomes] |
rs6794975 | 0.96[ASN][1000 genomes] |
rs6796339 | 0.96[ASN][1000 genomes] |
rs73146387 | 0.96[ASN][1000 genomes] |
rs7373232 | 0.99[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7374904 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9310110 | 0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9310112 | 0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9809894 | 0.99[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9829401 | 0.91[ASN][1000 genomes] |
rs9847087 | 0.91[ASN][1000 genomes] |
rs9848971 | 0.96[ASN][1000 genomes] |
rs9851954 | 0.91[ASN][1000 genomes] |
rs9852594 | 0.99[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9852981 | 0.89[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9862195 | 0.91[ASN][1000 genomes] |
rs9863058 | 0.87[ASN][1000 genomes] |
rs9866618 | 0.83[ASN][1000 genomes] |
rs9883541 | 0.91[ASN][1000 genomes] |
rs993186 | 0.87[ASN][1000 genomes] |
rs993187 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834760 | chr3:89085529-89299398 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv997874 | chr3:89188275-89279573 | Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv437866 | chr3:89247881-89480265 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:89250200-89263200 | Weak transcription | Fetal Brain Female | brain |
2 | chr3:89250400-89261800 | Weak transcription | Fetal Brain Male | brain |
3 | chr3:89251200-89259200 | Weak transcription | Fetal Muscle Leg | muscle |
4 | chr3:89255200-89259400 | Weak transcription | Brain Germinal Matrix | brain |