Variant report
Variant | rs7526396 |
---|---|
Chromosome Location | chr1:160900744-160900745 |
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] |
---|---|
rs11265522 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs11265526 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs11265533 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11265534 | 0.87[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs11265535 | 0.81[EUR][1000 genomes] |
rs11805631 | 0.88[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12126310 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1981048 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs2184066 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs28368883 | 0.84[EUR][1000 genomes] |
rs34655593 | 0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs3829790 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs3928803 | 0.82[EUR][1000 genomes] |
rs4656968 | 0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4656971 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs4656972 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs61802165 | 0.88[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6656769 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs6680969 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6691389 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs955615 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530077 | chr1:160836448-161284904 | Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 119 gene(s) | inside rSNPs | diseases |
2 | esv3430322 | chr1:160851829-160920480 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv947200 | chr1:160870136-160905390 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:160899800-160905400 | Weak transcription | Right Atrium | heart |