Variant report
Variant | rs7693587 |
---|---|
Chromosome Location | chr4:62418913-62418914 |
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[EUR][1000 genomes] |
rs10517536 | 1.00[EUR][1000 genomes] |
rs10517540 | 1.00[AMR][1000 genomes] |
rs11131326 | 1.00[EUR][1000 genomes] |
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] |
rs1497903 | 1.00[AMR][1000 genomes] |
rs1497904 | 1.00[EUR][1000 genomes] |
rs1531204 | 1.00[EUR][1000 genomes] |
rs17081925 | 1.00[AMR][1000 genomes] |
rs17090502 | 1.00[EUR][1000 genomes] |
rs17090511 | 1.00[EUR][1000 genomes] |
rs17090512 | 1.00[EUR][1000 genomes] |
rs17090513 | 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[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] |
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[EUR][1000 genomes] |
rs335281 | 1.00[EUR][1000 genomes] |
rs335283 | 1.00[EUR][1000 genomes] |
rs335284 | 1.00[EUR][1000 genomes] |
rs335293 | 1.00[EUR][1000 genomes] |
rs335297 | 1.00[EUR][1000 genomes] |
rs335298 | 1.00[EUR][1000 genomes] |
rs335326 | 1.00[EUR][1000 genomes] |
rs335327 | 1.00[EUR][1000 genomes] |
rs335328 | 1.00[EUR][1000 genomes] |
rs335330 | 1.00[EUR][1000 genomes] |
rs335331 | 1.00[EUR][1000 genomes] |
rs335333 | 1.00[EUR][1000 genomes] |
rs335339 | 1.00[EUR][1000 genomes] |
rs335340 | 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] |
rs58496049 | 1.00[AMR][1000 genomes] |
rs60090447 | 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[EUR][1000 genomes] |
rs7655377 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7660777 | 1.00[EUR][1000 genomes] |
rs7683598 | 1.00[EUR][1000 genomes] |
rs7693679 | 1.00[EUR][1000 genomes] |
rs7698624 | 1.00[EUR][1000 genomes] |
rs954164 | 1.00[AMR][1000 genomes] |
rs9654273 | 1.00[EUR][1000 genomes] |
rs991586 | 1.00[EUR][1000 genomes] |
rs991587 | 1.00[EUR][1000 genomes] |
rs991588 | 1.00[EUR][1000 genomes] |
rs9968259 | 1.00[AMR][1000 genomes] |
rs9968477 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | 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 |
2 | 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 |
3 | nsv461377 | chr4:62368762-62883431 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv594328 | chr4:62368762-62883431 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1004815 | chr4:62398737-62553769 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv537110 | chr4:62398737-62553769 | ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1004432 | chr4:62408333-62444506 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
8 | nsv537111 | chr4:62408333-62444506 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
9 | nsv594329 | chr4:62416593-62478230 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:62407000-62421600 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr4:62408000-62421200 | Weak transcription | Fetal Intestine Small | intestine |
3 | chr4:62409600-62419200 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
4 | chr4:62415200-62421600 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
5 | chr4:62416800-62421200 | Weak transcription | Small Intestine | intestine |
6 | chr4:62417000-62421000 | Weak transcription | Fetal Heart | heart |
7 | chr4:62417400-62420800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
8 | chr4:62418800-62419600 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
9 | chr4:62418800-62419600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |