Variant report
Variant | rs8003236 |
---|---|
Chromosome Location | chr14:25538445-25538446 |
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 | 0.87[ASN][1000 genomes] |
rs10147992 | 0.95[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes] |
rs11159034 | 0.83[CHB][hapmap] |
rs11159041 | 0.84[ASN][1000 genomes] |
rs11846310 | 0.85[EUR][1000 genomes] |
rs11847320 | 0.81[ASN][1000 genomes] |
rs12433556 | 0.85[EUR][1000 genomes] |
rs1952497 | 0.85[EUR][1000 genomes] |
rs1952498 | 0.85[EUR][1000 genomes] |
rs28445295 | 0.83[EUR][1000 genomes] |
rs59800591 | 0.85[EUR][1000 genomes] |
rs6574173 | 0.83[AFR][1000 genomes] |
rs7147583 | 0.99[ASN][1000 genomes] |
rs7158626 | 0.96[ASN][1000 genomes] |
rs726519 | 0.92[CEU][hapmap] |
rs729368 | 0.92[ASN][1000 genomes] |
rs8007508 | 0.85[AFR][1000 genomes] |
rs8014755 | 0.99[ASN][1000 genomes] |
rs8020392 | 0.92[CEU][hapmap] |
rs873102 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs912304 | 0.83[CHB][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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:25537400-25539800 | Enhancers | Fetal Muscle Leg | muscle |