Variant report
Variant | rs335327 |
---|---|
Chromosome Location | chr4:62345024-62345025 |
allele | A/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] |
---|---|
rs1037671 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs10517536 | 1.00[EUR][1000 genomes] |
rs11131326 | 1.00[EUR][1000 genomes] |
rs11131330 | 1.00[MEX][hapmap] |
rs1350247 | 1.00[EUR][1000 genomes] |
rs1379167 | 1.00[EUR][1000 genomes] |
rs1456867 | 1.00[EUR][1000 genomes] |
rs1456875 | 1.00[EUR][1000 genomes] |
rs1456876 | 1.00[EUR][1000 genomes] |
rs1456877 | 1.00[EUR][1000 genomes] |
rs1456878 | 1.00[EUR][1000 genomes] |
rs1497902 | 1.00[EUR][1000 genomes] |
rs1497904 | 1.00[EUR][1000 genomes] |
rs1497917 | 1.00[TSI][hapmap] |
rs1531204 | 1.00[EUR][1000 genomes] |
rs17090502 | 1.00[EUR][1000 genomes] |
rs17090511 | 1.00[EUR][1000 genomes] |
rs17090512 | 1.00[EUR][1000 genomes] |
rs17090513 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs1845582 | 1.00[EUR][1000 genomes] |
rs2124795 | 1.00[EUR][1000 genomes] |
rs2124796 | 1.00[EUR][1000 genomes] |
rs2219342 | 1.00[EUR][1000 genomes] |
rs2606712 | 1.00[EUR][1000 genomes] |
rs2606714 | 1.00[EUR][1000 genomes] |
rs2606715 | 1.00[EUR][1000 genomes] |
rs2606716 | 1.00[EUR][1000 genomes] |
rs2606717 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs2606718 | 1.00[EUR][1000 genomes] |
rs2606720 | 1.00[EUR][1000 genomes] |
rs2643035 | 1.00[EUR][1000 genomes] |
rs2643037 | 1.00[EUR][1000 genomes] |
rs2643038 | 1.00[EUR][1000 genomes] |
rs2643039 | 1.00[EUR][1000 genomes] |
rs2643040 | 1.00[EUR][1000 genomes] |
rs335270 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes] |
rs335274 | 1.00[EUR][1000 genomes] |
rs335275 | 1.00[EUR][1000 genomes] |
rs335276 | 1.00[EUR][1000 genomes] |
rs335277 | 1.00[EUR][1000 genomes] |
rs335278 | 1.00[EUR][1000 genomes] |
rs335280 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs335281 | 1.00[EUR][1000 genomes] |
rs335283 | 1.00[EUR][1000 genomes] |
rs335284 | 1.00[EUR][1000 genomes] |
rs335293 | 1.00[ASW][hapmap];0.97[LWK][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335297 | 0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335298 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335326 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335328 | 1.00[ASW][hapmap];0.97[LWK][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335330 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335331 | 0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335333 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs335339 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs335340 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs335343 | 1.00[EUR][1000 genomes] |
rs335344 | 1.00[EUR][1000 genomes] |
rs335345 | 1.00[EUR][1000 genomes] |
rs335346 | 1.00[EUR][1000 genomes] |
rs335347 | 1.00[EUR][1000 genomes] |
rs335348 | 1.00[EUR][1000 genomes] |
rs4860413 | 1.00[EUR][1000 genomes] |
rs6551630 | 1.00[EUR][1000 genomes] |
rs6814707 | 1.00[EUR][1000 genomes] |
rs6823672 | 1.00[EUR][1000 genomes] |
rs6834543 | 1.00[EUR][1000 genomes] |
rs6841033 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs6856328 | 1.00[TSI][hapmap] |
rs7655377 | 1.00[EUR][1000 genomes] |
rs7660777 | 1.00[EUR][1000 genomes] |
rs7666147 | 1.00[MEX][hapmap] |
rs7678777 | 1.00[MEX][hapmap] |
rs7683598 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs7687816 | 1.00[TSI][hapmap] |
rs7693587 | 1.00[EUR][1000 genomes] |
rs7693679 | 1.00[EUR][1000 genomes] |
rs7698624 | 1.00[EUR][1000 genomes] |
rs9654273 | 1.00[EUR][1000 genomes] |
rs987749 | 1.00[MEX][hapmap] |
rs991586 | 1.00[EUR][1000 genomes] |
rs991587 | 1.00[EUR][1000 genomes] |
rs991588 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs9998456 | 1.00[MEX][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv879075 | chr4:62124531-62354791 | Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv868844 | chr4:62241702-62497248 | Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv879076 | chr4:62251077-62354791 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2753138 | chr4:62271444-62442507 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1005770 | chr4:62344379-62398798 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv537109 | chr4:62344379-62398798 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:62341200-62348000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |