Variant report
Variant | rs72912494 |
---|---|
Chromosome Location | chr18:44919365-44919366 |
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] |
---|---|
rs55687418 | 1.00[ASN][1000 genomes] |
rs55698938 | 1.00[ASN][1000 genomes] |
rs55813572 | 1.00[ASN][1000 genomes] |
rs55825078 | 1.00[ASN][1000 genomes] |
rs55892143 | 1.00[ASN][1000 genomes] |
rs56077098 | 1.00[ASN][1000 genomes] |
rs56109704 | 1.00[ASN][1000 genomes] |
rs56287570 | 1.00[ASN][1000 genomes] |
rs58684150 | 1.00[ASN][1000 genomes] |
rs66485937 | 1.00[ASN][1000 genomes] |
rs66914705 | 1.00[ASN][1000 genomes] |
rs67119810 | 1.00[ASN][1000 genomes] |
rs67123015 | 1.00[ASN][1000 genomes] |
rs67514853 | 1.00[ASN][1000 genomes] |
rs67822267 | 1.00[ASN][1000 genomes] |
rs72908572 | 1.00[ASN][1000 genomes] |
rs72908575 | 1.00[ASN][1000 genomes] |
rs72908588 | 1.00[ASN][1000 genomes] |
rs72909289 | 1.00[ASN][1000 genomes] |
rs72910504 | 1.00[ASN][1000 genomes] |
rs72910505 | 1.00[ASN][1000 genomes] |
rs72910507 | 1.00[ASN][1000 genomes] |
rs72910512 | 1.00[ASN][1000 genomes] |
rs72910513 | 1.00[ASN][1000 genomes] |
rs72910516 | 1.00[ASN][1000 genomes] |
rs72910538 | 1.00[ASN][1000 genomes] |
rs72910544 | 1.00[ASN][1000 genomes] |
rs72910547 | 1.00[ASN][1000 genomes] |
rs72910552 | 1.00[ASN][1000 genomes] |
rs72910554 | 1.00[ASN][1000 genomes] |
rs72911203 | 1.00[ASN][1000 genomes] |
rs72911205 | 1.00[ASN][1000 genomes] |
rs72911207 | 1.00[ASN][1000 genomes] |
rs72912419 | 1.00[ASN][1000 genomes] |
rs72912427 | 1.00[ASN][1000 genomes] |
rs72912445 | 1.00[ASN][1000 genomes] |
rs72912456 | 1.00[ASN][1000 genomes] |
rs72912458 | 1.00[ASN][1000 genomes] |
rs72912473 | 1.00[ASN][1000 genomes] |
rs72912475 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72912490 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72913164 | 1.00[ASN][1000 genomes] |
rs72913166 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv833641 | chr18:44815063-45020202 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionChromatin interactive regionlncRNAmiRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv1801141 | chr18:44908270-44955409 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:44918200-44919400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |