Variant report
Variant | rs28719598 |
---|---|
Chromosome Location | chr8:10943884-10943885 |
allele | C/T |
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] |
---|---|
rs10091993 | 0.88[ASN][1000 genomes] |
rs10099881 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10108304 | 0.83[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10108618 | 0.85[ASN][1000 genomes] |
rs10109101 | 0.81[EUR][1000 genomes] |
rs10113735 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11986748 | 0.81[EUR][1000 genomes] |
rs11991121 | 0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11991716 | 0.85[ASN][1000 genomes] |
rs12542383 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs17723229 | 0.80[ASN][1000 genomes] |
rs2409694 | 0.85[ASN][1000 genomes] |
rs28510951 | 0.84[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs28722721 | 0.85[ASN][1000 genomes] |
rs2898258 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4262293 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4840542 | 0.85[ASN][1000 genomes] |
rs55676920 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs55813668 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs59724806 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs60134032 | 0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6601559 | 0.85[ASN][1000 genomes] |
rs6601560 | 0.85[ASN][1000 genomes] |
rs66475020 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6982381 | 0.85[ASN][1000 genomes] |
rs6999969 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7014291 | 0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7463505 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7812573 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7820860 | 0.85[ASN][1000 genomes] |
rs7835318 | 0.85[ASN][1000 genomes] |
rs9329235 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs9657519 | 0.85[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 | esv1815171 | chr8:10940039-11128712 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
4 | nsv1025426 | chr8:10942929-11037903 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:10925600-10944400 | Weak transcription | H9 Cell Line | embryonic stem cell |
2 | chr8:10942200-10944400 | Enhancers | Fetal Heart | heart |
3 | chr8:10943000-10948400 | Weak transcription | Gastric | stomach |
4 | chr8:10943800-10944200 | Enhancers | Brain Anterior Caudate | brain |