Variant report
Variant | rs7147583 |
---|---|
Chromosome Location | chr14:25536371-25536372 |
allele | A/G |
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] |
---|---|
rs10142533 | 0.86[ASN][1000 genomes] |
rs10147992 | 0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes] |
rs11159034 | 0.83[CHB][hapmap];0.86[CHD][hapmap] |
rs11159041 | 0.84[ASN][1000 genomes] |
rs11847320 | 0.81[ASN][1000 genomes] |
rs2004925 | 0.84[MKK][hapmap] |
rs2038700 | 0.81[ASW][hapmap] |
rs2332462 | 0.82[CHD][hapmap];0.84[MKK][hapmap] |
rs6574126 | 0.81[CHD][hapmap];0.86[MKK][hapmap] |
rs7141943 | 0.84[MKK][hapmap] |
rs7158626 | 0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs729368 | 0.93[ASN][1000 genomes] |
rs8003236 | 0.99[ASN][1000 genomes] |
rs8014755 | 0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs873102 | 0.81[ASW][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.98[MKK][hapmap];0.91[YRI][hapmap];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs912304 | 0.83[CHB][hapmap];0.86[CHD][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv901504 | chr14:25184210-25646203 | Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv901509 | chr14:25398571-25743484 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv901511 | chr14:25505085-25588029 | Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | esv15004 | chr14:25536352-25537322 | Enhancers | n/a | n/a | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:25535000-25536800 | Enhancers | Brain Germinal Matrix | brain |