Variant report
Variant | rs1336141 |
---|---|
Chromosome Location | chr13:63098996-63098997 |
allele | A/C |
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] |
---|---|
rs12428082 | 0.89[EUR][1000 genomes] |
rs12428375 | 0.89[EUR][1000 genomes] |
rs12428560 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12429317 | 0.89[EUR][1000 genomes] |
rs12429390 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12429397 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12429424 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12431026 | 0.89[EUR][1000 genomes] |
rs12431035 | 0.89[EUR][1000 genomes] |
rs12431064 | 0.89[EUR][1000 genomes] |
rs12862055 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12864625 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12867188 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12870231 | 0.89[EUR][1000 genomes] |
rs12870258 | 0.88[EUR][1000 genomes] |
rs12870727 | 0.82[EUR][1000 genomes] |
rs12870826 | 0.85[EUR][1000 genomes] |
rs12870935 | 0.82[EUR][1000 genomes] |
rs12871366 | 0.89[EUR][1000 genomes] |
rs12871694 | 0.82[EUR][1000 genomes] |
rs12872004 | 0.89[EUR][1000 genomes] |
rs12875940 | 0.89[EUR][1000 genomes] |
rs12876207 | 0.89[EUR][1000 genomes] |
rs12876281 | 0.87[EUR][1000 genomes] |
rs12876343 | 0.85[EUR][1000 genomes] |
rs12876465 | 0.89[EUR][1000 genomes] |
rs12876620 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12876700 | 0.89[EUR][1000 genomes] |
rs12876997 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12877105 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12877223 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12877330 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs17061308 | 0.89[EUR][1000 genomes] |
rs17298039 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs34824349 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs34909131 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35185476 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35491594 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35869046 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4438182 | 0.89[EUR][1000 genomes] |
rs4883682 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4884420 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4884421 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4884422 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4884423 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs71439933 | 0.89[EUR][1000 genomes] |
rs71439935 | 0.89[EUR][1000 genomes] |
rs71439947 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs71439948 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs71439955 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1038992 | chr13:62827929-63369497 | Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv541795 | chr13:62827929-63369497 | Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1038215 | chr13:62836702-63405446 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv561895 | chr13:63098996-63147070 | Flanking Active TSS Enhancers Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:63098400-63099400 | Flanking Active TSS | GM12878-XiMat | blood |
2 | chr13:63098600-63099000 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr13:63098600-63099200 | Enhancers | H1 Cell Line | embryonic stem cell |
4 | chr13:63098600-63099400 | Enhancers | H9 Cell Line | embryonic stem cell |
5 | chr13:63098800-63099400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |