Variant report
Variant | rs7158379 |
---|---|
Chromosome Location | chr14:79898506-79898507 |
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] |
---|---|
rs11848998 | 0.85[GIH][hapmap];1.00[TSI][hapmap] |
rs12436858 | 0.86[JPT][hapmap];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs17109172 | 1.00[TSI][hapmap] |
rs17109214 | 0.87[YRI][hapmap] |
rs17109218 | 1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap] |
rs17109224 | 1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs56187621 | 1.00[AMR][1000 genomes] |
rs56376412 | 1.00[AMR][1000 genomes] |
rs57309646 | 1.00[AMR][1000 genomes] |
rs6574504 | 1.00[TSI][hapmap] |
rs7144015 | 1.00[TSI][hapmap] |
rs73339468 | 1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs74068628 | 1.00[AMR][1000 genomes] |
rs74068669 | 1.00[AMR][1000 genomes] |
rs74068675 | 1.00[AMR][1000 genomes] |
rs74068676 | 1.00[AMR][1000 genomes] |
rs74068677 | 1.00[AMR][1000 genomes] |
rs74068679 | 1.00[AMR][1000 genomes] |
rs74068693 | 1.00[AMR][1000 genomes] |
rs8005044 | 1.00[TSI][hapmap] |
rs8014580 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv931412 | chr14:79420297-79928269 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv902110 | chr14:79624492-79998294 | Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv530072 | chr14:79769657-79928269 | Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1045241 | chr14:79885361-80734201 | Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:79884200-79901800 | Weak transcription | Stomach Smooth Muscle | stomach |