Variant report
Variant | rs59417246 |
---|---|
Chromosome Location | chr7:78084779-78084780 |
allele | A/G |
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] |
---|---|
rs10237632 | 0.87[EUR][1000 genomes] |
rs10260177 | 0.86[EUR][1000 genomes] |
rs10270014 | 0.87[EUR][1000 genomes] |
rs1157211 | 0.87[EUR][1000 genomes] |
rs17150823 | 0.82[EUR][1000 genomes] |
rs2302638 | 0.86[ASN][1000 genomes] |
rs2302639 | 0.86[ASN][1000 genomes] |
rs2302640 | 0.86[ASN][1000 genomes] |
rs2302641 | 0.85[ASN][1000 genomes] |
rs4314593 | 0.82[EUR][1000 genomes] |
rs4623346 | 0.82[EUR][1000 genomes] |
rs59370246 | 0.90[ASN][1000 genomes] |
rs59424961 | 0.86[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs73148383 | 0.81[EUR][1000 genomes] |
rs73148390 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs73148393 | 0.83[EUR][1000 genomes] |
rs7779438 | 0.99[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7786447 | 0.87[EUR][1000 genomes] |
rs7787781 | 0.86[EUR][1000 genomes] |
rs7791794 | 0.87[EUR][1000 genomes] |
rs7801490 | 0.85[ASN][1000 genomes] |
rs7801864 | 1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7803197 | 0.87[EUR][1000 genomes] |
rs7810530 | 0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1022764 | chr7:77911072-78316607 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1022199 | chr7:78054639-78469370 | Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv538986 | chr7:78054639-78469370 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:78083000-78088600 | Weak transcription | Brain Substantia Nigra | brain |