Variant report
Variant | rs31396 |
---|---|
Chromosome Location | chr14:79355306-79355307 |
allele | A/C |
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] |
---|---|
rs1509151 | 1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap] |
rs154299 | 1.00[CEU][hapmap];0.80[CHB][hapmap] |
rs154310 | 1.00[CEU][hapmap];0.81[AMR][1000 genomes] |
rs154314 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs17108324 | 0.86[CHB][hapmap] |
rs31357 | 1.00[CEU][hapmap];0.81[CHB][hapmap] |
rs31361 | 1.00[CEU][hapmap];0.80[CHB][hapmap] |
rs31363 | 1.00[CEU][hapmap];0.80[CHB][hapmap];0.81[AMR][1000 genomes] |
rs31393 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs31394 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs31395 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs39893 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs42568 | 1.00[CEU][hapmap];0.81[AMR][1000 genomes] |
rs60924894 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs74067145 | 0.93[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs749919 | 1.00[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832838 | chr14:79306627-79445382 | Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
2 | nsv1048274 | chr14:79323592-79417906 | Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |