Variant report
Variant | rs7825261 |
---|---|
Chromosome Location | chr8:42637683-42637684 |
allele | A/C |
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] |
---|---|
rs10087172 | 0.91[AMR][1000 genomes] |
rs10092346 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10105699 | 0.99[ASN][1000 genomes] |
rs10107450 | 0.83[AMR][1000 genomes] |
rs10108797 | 0.92[AMR][1000 genomes] |
rs10109040 | 0.91[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs10110332 | 0.84[AMR][1000 genomes] |
rs1072003 | 0.87[AMR][1000 genomes] |
rs11986893 | 0.82[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs11995030 | 0.91[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs1960346 | 0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2082591 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2117225 | 0.91[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs2196128 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2217732 | 0.88[AMR][1000 genomes] |
rs28501554 | 0.92[AMR][1000 genomes] |
rs28784665 | 0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs28826992 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs34996273 | 0.87[ASN][1000 genomes] |
rs4509313 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs4567031 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs4737068 | 0.91[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs4737071 | 0.82[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs56395510 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6474418 | 0.83[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs6474420 | 0.85[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs6984252 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs6999449 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7000412 | 0.88[AMR][1000 genomes] |
rs7001753 | 0.88[AMR][1000 genomes] |
rs7003968 | 1.00[ASN][1000 genomes] |
rs7005126 | 0.88[ASN][1000 genomes] |
rs7015935 | 0.86[AMR][1000 genomes] |
rs7826201 | 0.95[ASN][1000 genomes] |
rs7831096 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7841834 | 0.82[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs7845365 | 0.98[ASN][1000 genomes] |
rs892413 | 0.91[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530880 | chr8:41895241-42755506 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
2 | nsv1034724 | chr8:42386707-42772203 | Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 36 gene(s) | inside rSNPs | diseases |
3 | nsv428516 | chr8:42577171-42731235 | Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 18 gene(s) | inside rSNPs | diseases |
4 | nsv890846 | chr8:42625663-43240123 | Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 86 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:42637000-42639000 | Weak transcription | Pancreas | Pancrea |