Variant report
Variant | rs4235146 |
---|---|
Chromosome Location | chr4:47304860-47304861 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10000697 | 0.88[CEU][hapmap] |
rs10023965 | 0.88[CEU][hapmap] |
rs10440176 | 0.82[CEU][hapmap] |
rs11731871 | 0.86[CEU][hapmap] |
rs11929757 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs12331018 | 0.88[CEU][hapmap] |
rs12503495 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13108343 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13114985 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13129278 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17461709 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28595697 | 0.81[EUR][1000 genomes] |
rs34282295 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35276546 | 0.82[ASN][1000 genomes] |
rs3822112 | 0.85[CEU][hapmap] |
rs4261959 | 0.86[CEU][hapmap] |
rs4261968 | 0.86[CEU][hapmap] |
rs4302438 | 0.85[CEU][hapmap] |
rs4386575 | 0.84[CEU][hapmap] |
rs4495018 | 0.88[CEU][hapmap] |
rs4508859 | 1.00[JPT][hapmap] |
rs4518219 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4588429 | 0.84[CEU][hapmap] |
rs55818428 | 0.82[ASN][1000 genomes] |
rs6447546 | 0.88[CEU][hapmap] |
rs6831556 | 0.84[CEU][hapmap] |
rs73249609 | 0.82[ASN][1000 genomes] |
rs7665508 | 0.84[CEU][hapmap] |
rs7674333 | 0.92[CEU][hapmap] |
rs7687439 | 0.89[CEU][hapmap] |
rs9291305 | 0.88[CEU][hapmap] |
rs9683412 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs9917915 | 0.92[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv998919 | chr4:47207023-47476876 | Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv879004 | chr4:47234200-47322190 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:47303600-47305000 | Enhancers | Muscle Satellite Cultured Cells | -- |