Variant report
Variant | rs73435837 |
---|---|
Chromosome Location | chr6:49606757-49606758 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
1
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
RHAG | TF binding region |
rs_ID | r2[population] |
---|---|
rs10948530 | 1.00[EUR][1000 genomes] |
rs1268283 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1268284 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1268286 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1268797 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1270361 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1383377 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16879837 | 1.00[EUR][1000 genomes] |
rs2396908 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs35289289 | 1.00[EUR][1000 genomes] |
rs56994564 | 1.00[EUR][1000 genomes] |
rs57160213 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57295760 | 1.00[EUR][1000 genomes] |
rs57341323 | 1.00[EUR][1000 genomes] |
rs57400170 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57420263 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs57746041 | 1.00[EUR][1000 genomes] |
rs57968495 | 1.00[EUR][1000 genomes] |
rs58946005 | 1.00[EUR][1000 genomes] |
rs59784644 | 1.00[EUR][1000 genomes] |
rs59924621 | 1.00[EUR][1000 genomes] |
rs60493453 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60504565 | 1.00[EUR][1000 genomes] |
rs60669025 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60925322 | 1.00[EUR][1000 genomes] |
rs61273820 | 1.00[EUR][1000 genomes] |
rs61627916 | 1.00[EUR][1000 genomes] |
rs6458699 | 1.00[AMR][1000 genomes] |
rs6458700 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6458703 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6915891 | 1.00[AMR][1000 genomes] |
rs73423739 | 1.00[EUR][1000 genomes] |
rs73425837 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73425844 | 1.00[EUR][1000 genomes] |
rs73425861 | 1.00[EUR][1000 genomes] |
rs73433897 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435808 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435811 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435814 | 1.00[EUR][1000 genomes] |
rs73435828 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435853 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435867 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435869 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435872 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435876 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435899 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73435901 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73437803 | 1.00[EUR][1000 genomes] |
rs73437853 | 1.00[EUR][1000 genomes] |
rs73437860 | 1.00[EUR][1000 genomes] |
rs73437864 | 1.00[EUR][1000 genomes] |
rs73437867 | 1.00[EUR][1000 genomes] |
rs73437871 | 1.00[EUR][1000 genomes] |
rs73437872 | 1.00[EUR][1000 genomes] |
rs73437876 | 1.00[EUR][1000 genomes] |
rs73437878 | 1.00[EUR][1000 genomes] |
rs73437880 | 1.00[EUR][1000 genomes] |
rs73437882 | 1.00[EUR][1000 genomes] |
rs73437884 | 1.00[EUR][1000 genomes] |
rs73439848 | 1.00[EUR][1000 genomes] |
rs73439854 | 1.00[EUR][1000 genomes] |
rs73439856 | 1.00[EUR][1000 genomes] |
rs73439857 | 1.00[EUR][1000 genomes] |
rs73439862 | 1.00[EUR][1000 genomes] |
rs73439865 | 1.00[EUR][1000 genomes] |
rs73439869 | 1.00[EUR][1000 genomes] |
rs73439877 | 1.00[EUR][1000 genomes] |
rs73441811 | 1.00[EUR][1000 genomes] |
rs73441829 | 1.00[EUR][1000 genomes] |
rs73441834 | 1.00[EUR][1000 genomes] |
rs73441836 | 1.00[EUR][1000 genomes] |
rs73441840 | 1.00[EUR][1000 genomes] |
rs73441857 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1024959 | chr6:49290141-49652124 | Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv1021136 | chr6:49295037-49631278 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
3 | nsv933942 | chr6:49480550-50004231 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
4 | nsv933833 | chr6:49515134-49961765 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:49601800-49607000 | Weak transcription | HepG2 | liver |
2 | chr6:49606400-49607400 | Enhancers | K562 | blood |
3 | chr6:49606600-49607200 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr6:49606600-49607400 | Enhancers | Fetal Stomach | stomach |