Variant report
Variant | rs1491746 |
---|---|
Chromosome Location | chr3:68379240-68379241 |
allele | C/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] |
---|---|
rs10510969 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap] |
rs1352853 | 0.87[CEU][hapmap] |
rs1388506 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1388507 | 0.82[JPT][hapmap] |
rs1491748 | 0.86[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap] |
rs2313283 | 0.95[CEU][hapmap] |
rs262217 | 0.91[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap] |
rs262219 | 0.86[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap] |
rs262220 | 0.91[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap] |
rs262249 | 0.82[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes] |
rs262251 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs262252 | 0.91[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2665523 | 0.91[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap] |
rs4568137 | 0.82[JPT][hapmap] |
rs983963 | 0.82[JPT][hapmap] |
rs994553 | 0.82[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752014 | chr3:68091879-68416989 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1010992 | chr3:68353191-68388825 | Weak transcription Enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv834721 | chr3:68365963-68526394 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |