Variant report
Variant | rs12619688 |
---|---|
Chromosome Location | chr2:125473407-125473408 |
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] |
---|---|
rs10164548 | 0.81[ASN][1000 genomes] |
rs10178842 | 1.00[JPT][hapmap] |
rs10179213 | 1.00[JPT][hapmap] |
rs10183674 | 1.00[JPT][hapmap];0.81[ASN][1000 genomes] |
rs10184800 | 1.00[JPT][hapmap] |
rs10185492 | 1.00[JPT][hapmap] |
rs10208814 | 0.82[JPT][hapmap] |
rs11123062 | 1.00[JPT][hapmap] |
rs11680115 | 1.00[JPT][hapmap] |
rs11694621 | 0.81[ASN][1000 genomes] |
rs12468133 | 1.00[JPT][hapmap] |
rs12992994 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13021629 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13386677 | 0.81[ASN][1000 genomes] |
rs13396871 | 1.00[JPT][hapmap] |
rs13400133 | 1.00[JPT][hapmap];0.81[ASN][1000 genomes] |
rs13406974 | 0.81[ASN][1000 genomes] |
rs13409512 | 1.00[JPT][hapmap] |
rs13427244 | 1.00[JPT][hapmap] |
rs6713505 | 1.00[JPT][hapmap];0.81[ASN][1000 genomes] |
rs6736347 | 1.00[JPT][hapmap];0.81[ASN][1000 genomes] |
rs6760383 | 1.00[JPT][hapmap] |
rs717601 | 1.00[JPT][hapmap] |
rs730468 | 1.00[JPT][hapmap];0.81[ASN][1000 genomes] |
rs7582461 | 0.82[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834359 | chr2:125367872-125536022 | Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
2 | nsv428727 | chr2:125372897-125512949 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
No data |