Variant report
Variant | rs73541296 |
---|---|
Chromosome Location | chr8:10899702-10899703 |
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] |
---|---|
rs10102241 | 0.90[ASN][1000 genomes] |
rs11996027 | 0.82[ASN][1000 genomes] |
rs12335200 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17152785 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17152791 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17152793 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17152795 | 1.00[ASN][1000 genomes] |
rs17155406 | 0.90[ASN][1000 genomes] |
rs35539607 | 0.90[ASN][1000 genomes] |
rs36088662 | 0.90[ASN][1000 genomes] |
rs4141827 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56665484 | 0.90[ASN][1000 genomes] |
rs59008721 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60039934 | 0.82[ASN][1000 genomes] |
rs60514110 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60680986 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61027371 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6601548 | 0.90[ASN][1000 genomes] |
rs6601549 | 0.90[ASN][1000 genomes] |
rs7015045 | 0.90[ASN][1000 genomes] |
rs73541252 | 0.90[ASN][1000 genomes] |
rs73541270 | 1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs73541286 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73541293 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73541300 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73541301 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1035072 | chr8:10819444-11480692 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
2 | nsv539473 | chr8:10819444-11480692 | Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
3 | nsv1022434 | chr8:10866242-10916523 | Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:10889800-10910800 | Weak transcription | HSMMtube | muscle |
2 | chr8:10897400-10905600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |