Variant report
Variant | rs72735391 |
---|---|
Chromosome Location | chr9:93440550-93440551 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr9:93440411..93442575-chr9:93562498..93565446,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000165025 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1542479 | 0.83[ASN][1000 genomes] |
rs16906728 | 0.90[ASN][1000 genomes] |
rs2297353 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2297354 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72733262 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72735386 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72735388 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72735390 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72735392 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72735395 | 0.87[ASN][1000 genomes] |
rs72744799 | 0.86[ASN][1000 genomes] |
rs72744801 | 0.86[ASN][1000 genomes] |
rs72746503 | 0.86[ASN][1000 genomes] |
rs72746505 | 0.86[ASN][1000 genomes] |
rs72746506 | 0.81[ASN][1000 genomes] |
rs72746508 | 0.86[ASN][1000 genomes] |
rs72746510 | 0.86[ASN][1000 genomes] |
rs72757615 | 0.86[ASN][1000 genomes] |
rs72757616 | 0.86[ASN][1000 genomes] |
rs72757617 | 0.86[ASN][1000 genomes] |
rs72757620 | 0.86[ASN][1000 genomes] |
rs72757623 | 0.88[ASN][1000 genomes] |
rs72757626 | 0.94[ASN][1000 genomes] |
rs72757629 | 0.94[ASN][1000 genomes] |
rs72757630 | 0.94[ASN][1000 genomes] |
rs72757631 | 0.94[ASN][1000 genomes] |
rs72757639 | 0.92[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1041278 | chr9:92965701-93560454 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1046989 | chr9:93353987-93800416 | Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv482757 | chr9:93356095-93543903 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv6610 | chr9:93428408-93473346 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:93439800-93440600 | Enhancers | Primary neutrophils fromperipheralblood | blood |