Variant report
Variant | rs73256306 |
---|---|
Chromosome Location | chr5:113335947-113335948 |
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] |
---|---|
rs13187234 | 1.00[EUR][1000 genomes] |
rs17136194 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17136271 | 1.00[EUR][1000 genomes] |
rs17136278 | 1.00[EUR][1000 genomes] |
rs2974457 | 1.00[EUR][1000 genomes] |
rs56823850 | 1.00[EUR][1000 genomes] |
rs57178641 | 1.00[EUR][1000 genomes] |
rs61188125 | 0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6867558 | 1.00[EUR][1000 genomes] |
rs6876006 | 1.00[EUR][1000 genomes] |
rs6881490 | 1.00[EUR][1000 genomes] |
rs6885474 | 1.00[EUR][1000 genomes] |
rs6885883 | 1.00[EUR][1000 genomes] |
rs73243066 | 1.00[EUR][1000 genomes] |
rs73243069 | 1.00[EUR][1000 genomes] |
rs73256373 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73779586 | 1.00[EUR][1000 genomes] |
rs73779601 | 1.00[EUR][1000 genomes] |
rs73782123 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7703903 | 1.00[EUR][1000 genomes] |
rs7716446 | 1.00[EUR][1000 genomes] |
rs7724198 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv471042 | chr5:113160490-113440892 | Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv599418 | chr5:113327561-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
3 | nsv599419 | chr5:113327561-113339698 | Enhancers | n/a | n/a | inside rSNPs | diseases |
4 | nsv599423 | chr5:113330738-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
5 | nsv599427 | chr5:113330990-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
6 | nsv599428 | chr5:113331136-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
7 | nsv599429 | chr5:113331281-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
8 | nsv599430 | chr5:113331546-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
9 | nsv599431 | chr5:113331616-113336598 | Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:113335200-113336200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |