Variant report
Variant | rs56976748 |
---|---|
Chromosome Location | chr3:54650990-54650991 |
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] |
---|---|
rs10510769 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10510770 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10510772 | 1.00[ASN][1000 genomes] |
rs1130197 | 1.00[ASN][1000 genomes] |
rs11914640 | 1.00[ASN][1000 genomes] |
rs11914780 | 1.00[ASN][1000 genomes] |
rs11924275 | 1.00[ASN][1000 genomes] |
rs12185982 | 1.00[ASN][1000 genomes] |
rs1427774 | 1.00[ASN][1000 genomes] |
rs17054227 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17054246 | 1.00[ASN][1000 genomes] |
rs17054250 | 1.00[ASN][1000 genomes] |
rs17054340 | 1.00[ASN][1000 genomes] |
rs17815617 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17816548 | 1.00[ASN][1000 genomes] |
rs17816566 | 1.00[ASN][1000 genomes] |
rs1863858 | 1.00[ASN][1000 genomes] |
rs2359857 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs28455661 | 1.00[ASN][1000 genomes] |
rs2884808 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34478567 | 1.00[ASN][1000 genomes] |
rs41381544 | 1.00[ASN][1000 genomes] |
rs4345041 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4386460 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55675480 | 1.00[ASN][1000 genomes] |
rs55772258 | 1.00[ASN][1000 genomes] |
rs55779022 | 0.86[EUR][1000 genomes] |
rs56008232 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56091855 | 0.86[EUR][1000 genomes] |
rs56112781 | 1.00[ASN][1000 genomes] |
rs56209938 | 1.00[ASN][1000 genomes] |
rs56260111 | 0.85[EUR][1000 genomes] |
rs56356828 | 0.84[EUR][1000 genomes] |
rs57924227 | 1.00[ASN][1000 genomes] |
rs58295654 | 1.00[ASN][1000 genomes] |
rs59004379 | 1.00[ASN][1000 genomes] |
rs62255527 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62255532 | 0.86[EUR][1000 genomes] |
rs62255533 | 1.00[ASN][1000 genomes] |
rs62255534 | 1.00[ASN][1000 genomes] |
rs62255535 | 1.00[ASN][1000 genomes] |
rs62255536 | 1.00[ASN][1000 genomes] |
rs62255538 | 1.00[ASN][1000 genomes] |
rs6803005 | 1.00[ASN][1000 genomes] |
rs72870661 | 1.00[ASN][1000 genomes] |
rs72870676 | 1.00[ASN][1000 genomes] |
rs72870688 | 1.00[ASN][1000 genomes] |
rs72872218 | 1.00[ASN][1000 genomes] |
rs72872226 | 1.00[ASN][1000 genomes] |
rs72872229 | 1.00[ASN][1000 genomes] |
rs72872244 | 1.00[ASN][1000 genomes] |
rs72872259 | 1.00[ASN][1000 genomes] |
rs72872285 | 1.00[ASN][1000 genomes] |
rs72874203 | 1.00[ASN][1000 genomes] |
rs72874204 | 1.00[ASN][1000 genomes] |
rs73068445 | 1.00[ASN][1000 genomes] |
rs7624695 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014595 | chr3:53944473-54846754 | Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv428084 | chr3:54404258-54742756 | Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv834700 | chr3:54637374-54803896 | Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:54646800-54655200 | Weak transcription | Brain Angular Gyrus | brain |
2 | chr3:54650400-54654600 | Weak transcription | Fetal Muscle Trunk | muscle |