Variant report
Variant | rs1965481 |
---|---|
Chromosome Location | chr7:99414919-99414920 |
allele | C/T |
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 |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000261511 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10255255 | 1.00[EUR][1000 genomes] |
rs10275362 | 1.00[EUR][1000 genomes] |
rs17161786 | 1.00[EUR][1000 genomes] |
rs2015504 | 1.00[EUR][1000 genomes] |
rs2404767 | 1.00[EUR][1000 genomes] |
rs2687089 | 0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2687095 | 1.00[EUR][1000 genomes] |
rs2687102 | 1.00[EUR][1000 genomes] |
rs2687103 | 1.00[EUR][1000 genomes] |
rs2687107 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs2687110 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs2687127 | 1.00[EUR][1000 genomes] |
rs2737418 | 1.00[EUR][1000 genomes] |
rs2738258 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs2740570 | 0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28808927 | 1.00[EUR][1000 genomes] |
rs28988585 | 1.00[EUR][1000 genomes] |
rs34314536 | 1.00[EUR][1000 genomes] |
rs34402397 | 1.00[EUR][1000 genomes] |
rs41300737 | 1.00[EUR][1000 genomes] |
rs41303946 | 1.00[EUR][1000 genomes] |
rs493380 | 1.00[EUR][1000 genomes] |
rs4986911 | 1.00[EUR][1000 genomes] |
rs56337765 | 1.00[EUR][1000 genomes] |
rs58679015 | 1.00[EUR][1000 genomes] |
rs58750403 | 1.00[EUR][1000 genomes] |
rs73408563 | 1.00[EUR][1000 genomes] |
rs73408565 | 1.00[EUR][1000 genomes] |
rs73711661 | 1.00[EUR][1000 genomes] |
rs73711662 | 1.00[EUR][1000 genomes] |
rs73711666 | 1.00[EUR][1000 genomes] |
rs73711671 | 1.00[EUR][1000 genomes] |
rs73711677 | 1.00[EUR][1000 genomes] |
rs73711681 | 1.00[EUR][1000 genomes] |
rs73711684 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1827709 | chr7:99353500-99440051 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | nsv970418 | chr7:99413271-99420442 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer | TF binding regionChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |