Variant report
Variant | rs7024275 |
---|---|
Chromosome Location | chr9:85698493-85698494 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10114832 | 0.81[EUR][1000 genomes] |
rs10117194 | 0.93[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs10120451 | 0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10867928 | 0.81[JPT][hapmap] |
rs10867930 | 0.80[CHB][hapmap] |
rs1393563 | 0.81[JPT][hapmap] |
rs1502687 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1542902 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1910261 | 0.81[EUR][1000 genomes] |
rs2378646 | 0.80[AMR][1000 genomes] |
rs4146961 | 0.81[JPT][hapmap] |
rs4301515 | 0.80[JPT][hapmap] |
rs4607702 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4877726 | 0.80[CHB][hapmap] |
rs6559696 | 0.90[AFR][1000 genomes] |
rs6559699 | 0.81[EUR][1000 genomes] |
rs7043558 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7849567 | 0.81[EUR][1000 genomes] |
rs7849682 | 0.81[EUR][1000 genomes] |
rs7849919 | 0.81[EUR][1000 genomes] |
rs7849921 | 0.81[EUR][1000 genomes] |
rs7855133 | 0.91[AFR][1000 genomes] |
rs7875431 | 0.81[EUR][1000 genomes] |
rs9942879 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9942922 | 0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv893511 | chr9:85495968-85833127 | Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1043722 | chr9:85663674-85747562 | Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv831642 | chr9:85679425-85817338 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv831643 | chr9:85679431-85798990 | Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:85682400-85706200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |