Variant report
Variant | rs1701986 |
---|---|
Chromosome Location | chr1:119191396-119191397 |
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] |
---|---|
rs1146303 | 0.81[EUR][1000 genomes] |
rs1213850 | 0.81[EUR][1000 genomes] |
rs1213851 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1213852 | 0.81[EUR][1000 genomes] |
rs1237215 | 0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1237971 | 0.81[EUR][1000 genomes] |
rs1358861 | 0.82[EUR][1000 genomes] |
rs1701970 | 0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1701975 | 0.82[EUR][1000 genomes] |
rs1701976 | 0.81[EUR][1000 genomes] |
rs1701983 | 0.82[EUR][1000 genomes] |
rs1742835 | 0.81[EUR][1000 genomes] |
rs1742837 | 0.81[EUR][1000 genomes] |
rs1742838 | 0.82[EUR][1000 genomes] |
rs1742839 | 0.82[EUR][1000 genomes] |
rs1742848 | 0.80[EUR][1000 genomes] |
rs2202581 | 0.81[EUR][1000 genomes] |
rs2659210 | 0.82[EUR][1000 genomes] |
rs2755132 | 0.80[EUR][1000 genomes] |
rs4233452 | 0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7550522 | 0.80[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3494191 | chr1:118772550-119719548 | Enhancers Strong transcription Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | esv3494192 | chr1:118772550-119719548 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:119190800-119194200 | Enhancers | Fetal Heart | heart |