Variant report
Variant | rs11941568 |
---|---|
Chromosome Location | chr4:57761839-57761840 |
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] |
---|---|
rs10030913 | 0.89[EUR][1000 genomes] |
rs10866440 | 0.89[EUR][1000 genomes] |
rs11730525 | 0.90[EUR][1000 genomes] |
rs11734953 | 0.86[EUR][1000 genomes] |
rs11933908 | 0.90[EUR][1000 genomes] |
rs12500454 | 0.80[EUR][1000 genomes] |
rs13108245 | 0.87[EUR][1000 genomes] |
rs13113802 | 0.87[EUR][1000 genomes] |
rs13146960 | 0.85[EUR][1000 genomes] |
rs13149162 | 0.91[EUR][1000 genomes] |
rs1877669 | 0.91[EUR][1000 genomes] |
rs2090962 | 0.92[EUR][1000 genomes] |
rs3000 | 0.90[EUR][1000 genomes] |
rs4864607 | 0.88[EUR][1000 genomes] |
rs6554397 | 0.89[EUR][1000 genomes] |
rs6554398 | 0.88[EUR][1000 genomes] |
rs6838948 | 0.90[EUR][1000 genomes] |
rs6854420 | 0.91[EUR][1000 genomes] |
rs6855212 | 0.94[EUR][1000 genomes] |
rs7666804 | 0.90[EUR][1000 genomes] |
rs7667302 | 0.90[EUR][1000 genomes] |
rs7667744 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7695970 | 0.91[EUR][1000 genomes] |
rs899630 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs899631 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs899632 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv868815 | chr4:57114268-58084688 | Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 88 gene(s) | inside rSNPs | diseases |
2 | nsv1012287 | chr4:57652778-57853485 | Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
3 | nsv1012125 | chr4:57668229-57865803 | Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:57761600-57773000 | Weak transcription | Right Atrium | heart |