Variant report
Variant | rs17359173 |
---|---|
Chromosome Location | chr4:175388082-175388083 |
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 |
No data |
(count:2 , 50 per page) page:
1
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rs_ID | r2[population] |
---|---|
rs10520284 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10520285 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17060524 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17060532 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17060537 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17060547 | 0.84[EUR][1000 genomes] |
rs17060557 | 0.84[EUR][1000 genomes] |
rs17294569 | 1.00[AFR][1000 genomes] |
rs17294646 | 1.00[AFR][1000 genomes] |
rs17358909 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17359381 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17360116 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs45445797 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs45446798 | 0.84[EUR][1000 genomes] |
rs45455595 | 1.00[AFR][1000 genomes] |
rs45471401 | 0.84[EUR][1000 genomes] |
rs45498507 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs45499501 | 1.00[AFR][1000 genomes] |
rs45548931 | 1.00[AFR][1000 genomes] |
rs45567139 | 1.00[AFR][1000 genomes] |
rs45592532 | 1.00[AFR][1000 genomes] |
rs45624235 | 1.00[AFR][1000 genomes] |
rs4613543 | 0.80[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869116 | chr4:175231090-175801761 | Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:175383600-175388200 | Weak transcription | Muscle Satellite Cultured Cells | -- |