Variant report
Variant | rs262219 |
---|---|
Chromosome Location | chr3:68396650-68396651 |
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] |
---|---|
rs10510969 | 0.86[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap] |
rs1352853 | 1.00[CEU][hapmap] |
rs1388500 | 0.85[YRI][hapmap] |
rs1388506 | 0.82[AMR][1000 genomes] |
rs1491746 | 0.86[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap] |
rs1491748 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs1510354 | 0.82[YRI][hapmap] |
rs2313283 | 0.90[CEU][hapmap] |
rs262215 | 0.82[YRI][hapmap] |
rs262217 | 0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs262220 | 0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs262249 | 0.81[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs262251 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs262252 | 0.95[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2665523 | 0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap] |
rs6549118 | 0.86[YRI][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 | nsv834721 | chr3:68365963-68526394 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv590562 | chr3:68393781-68422687 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |