Variant report
Variant | rs73078547 |
---|---|
Chromosome Location | chr3:56224807-56224808 |
allele | G/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] |
---|---|
rs1023882 | 1.00[ASN][1000 genomes] |
rs1317750 | 1.00[ASN][1000 genomes] |
rs55926504 | 1.00[ASN][1000 genomes] |
rs55968316 | 1.00[ASN][1000 genomes] |
rs56132867 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56138618 | 1.00[ASN][1000 genomes] |
rs56216904 | 1.00[ASN][1000 genomes] |
rs56227347 | 1.00[ASN][1000 genomes] |
rs56283068 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56286622 | 1.00[ASN][1000 genomes] |
rs56304204 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56317923 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56354761 | 1.00[ASN][1000 genomes] |
rs56383777 | 1.00[ASN][1000 genomes] |
rs56988974 | 1.00[ASN][1000 genomes] |
rs57708875 | 1.00[ASN][1000 genomes] |
rs58067804 | 1.00[ASN][1000 genomes] |
rs58449031 | 1.00[ASN][1000 genomes] |
rs58720638 | 1.00[ASN][1000 genomes] |
rs59412382 | 1.00[ASN][1000 genomes] |
rs59923603 | 1.00[ASN][1000 genomes] |
rs60120946 | 1.00[ASN][1000 genomes] |
rs60419369 | 1.00[ASN][1000 genomes] |
rs61092323 | 1.00[ASN][1000 genomes] |
rs61163420 | 1.00[ASN][1000 genomes] |
rs61248828 | 1.00[ASN][1000 genomes] |
rs61524165 | 1.00[ASN][1000 genomes] |
rs6802166 | 1.00[ASN][1000 genomes] |
rs73072703 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73072704 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73073904 | 1.00[ASN][1000 genomes] |
rs73073905 | 1.00[ASN][1000 genomes] |
rs73073910 | 1.00[ASN][1000 genomes] |
rs73073974 | 1.00[ASN][1000 genomes] |
rs73073978 | 1.00[ASN][1000 genomes] |
rs73073985 | 1.00[ASN][1000 genomes] |
rs73073992 | 1.00[ASN][1000 genomes] |
rs73075823 | 1.00[ASN][1000 genomes] |
rs73075825 | 1.00[ASN][1000 genomes] |
rs73075831 | 1.00[ASN][1000 genomes] |
rs73075832 | 1.00[ASN][1000 genomes] |
rs73075858 | 1.00[ASN][1000 genomes] |
rs73075865 | 1.00[ASN][1000 genomes] |
rs73078455 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078456 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078458 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078461 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078464 | 1.00[ASN][1000 genomes] |
rs73078465 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078470 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078474 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078477 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078479 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078482 | 1.00[ASN][1000 genomes] |
rs73078483 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078485 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078488 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73078496 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73080405 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73080407 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73080408 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73082476 | 1.00[ASN][1000 genomes] |
rs73086422 | 1.00[ASN][1000 genomes] |
rs73086435 | 1.00[ASN][1000 genomes] |
rs73086436 | 1.00[ASN][1000 genomes] |
rs73086437 | 1.00[ASN][1000 genomes] |
rs73086439 | 1.00[ASN][1000 genomes] |
rs73086440 | 1.00[ASN][1000 genomes] |
rs73086441 | 1.00[ASN][1000 genomes] |
rs73086449 | 1.00[ASN][1000 genomes] |
rs73088517 | 1.00[ASN][1000 genomes] |
rs73088520 | 1.00[ASN][1000 genomes] |
rs73088522 | 1.00[ASN][1000 genomes] |
rs73088532 | 1.00[ASN][1000 genomes] |
rs73088534 | 1.00[ASN][1000 genomes] |
rs73089162 | 1.00[ASN][1000 genomes] |
rs73089166 | 1.00[ASN][1000 genomes] |
rs73089189 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73089267 | 1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73089280 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73090547 | 1.00[ASN][1000 genomes] |
rs73090555 | 1.00[ASN][1000 genomes] |
rs73090565 | 1.00[ASN][1000 genomes] |
rs73090570 | 1.00[ASN][1000 genomes] |
rs73090572 | 1.00[ASN][1000 genomes] |
rs73091043 | 1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091049 | 1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091050 | 1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091252 | 1.00[ASN][1000 genomes] |
rs73091253 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091256 | 1.00[ASN][1000 genomes] |
rs73091258 | 1.00[ASN][1000 genomes] |
rs73091259 | 1.00[ASN][1000 genomes] |
rs73091260 | 1.00[ASN][1000 genomes] |
rs73091265 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091267 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091268 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091269 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73091270 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7615413 | 1.00[ASN][1000 genomes] |
rs7634259 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs969242 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1009709 | chr3:56000827-56294945 | Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:56223800-56225400 | Weak transcription | HSMM | muscle |
2 | chr3:56224000-56225400 | Weak transcription | HSMMtube | muscle |
3 | chr3:56224200-56226000 | Enhancers | Fetal Intestine Large | intestine |
4 | chr3:56224200-56226000 | Enhancers | Fetal Intestine Small | intestine |
5 | chr3:56224600-56225000 | Enhancers | Duodenum Mucosa | Duodenum |