Variant report
Variant | rs4734539 |
---|---|
Chromosome Location | chr8:92396932-92396933 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10088043 | 1.00[JPT][hapmap] |
rs10102488 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10102673 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs10109254 | 1.00[JPT][hapmap] |
rs10808635 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13248522 | 1.00[JPT][hapmap] |
rs13274956 | 1.00[JPT][hapmap] |
rs13281702 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs1375246 | 1.00[JPT][hapmap] |
rs16912688 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs2197810 | 1.00[JPT][hapmap] |
rs2339303 | 1.00[JPT][hapmap] |
rs28683647 | 0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4543502 | 1.00[JPT][hapmap] |
rs6988446 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6993624 | 0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7818318 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7823182 | 1.00[JPT][hapmap] |
rs7828102 | 1.00[JPT][hapmap] |
rs921231 | 1.00[JPT][hapmap] |
rs921232 | 1.00[JPT][hapmap] |
rs921235 | 1.00[JPT][hapmap] |
rs9297893 | 1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028628 | chr8:91680968-92418954 | Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
2 | nsv539672 | chr8:91680968-92418954 | Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
3 | nsv891190 | chr8:92354921-92484872 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
4 | nsv523642 | chr8:92391870-92542963 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1 gene(s) | inside rSNPs | diseases |
No data |