Variant report
Variant | rs3860324 |
---|---|
Chromosome Location | chr1:221809552-221809553 |
allele | A/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] |
---|---|
rs1018334 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10442685 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10863640 | 0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs11118777 | 0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11118778 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12023780 | 0.92[CEU][hapmap];0.85[GIH][hapmap];0.91[MEX][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12026281 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12029530 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12029601 | 0.84[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12136513 | 0.90[AFR][1000 genomes] |
rs12748524 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12753128 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1879068 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1933268 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2176690 | 0.81[AFR][1000 genomes] |
rs2378461 | 0.90[AFR][1000 genomes] |
rs4436399 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs4450027 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs4484930 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6658414 | 0.84[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs6658755 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6663135 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6663415 | 0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6663637 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6666514 | 0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6677071 | 0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6697462 | 0.92[CEU][hapmap];0.85[GIH][hapmap];0.87[MEX][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7540426 | 0.83[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv997685 | chr1:220993527-221863416 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
2 | nsv535299 | chr1:220993527-221863416 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
3 | nsv873200 | chr1:221644180-221843191 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv1011037 | chr1:221756526-221809552 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:221806000-221811200 | Weak transcription | Fetal Heart | heart |
2 | chr1:221806200-221813600 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
3 | chr1:221809200-221811000 | Weak transcription | HMEC | breast |