Variant report
Variant | rs2760550 |
---|---|
Chromosome Location | chr20:16116624-16116625 |
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] |
---|---|
rs1323304 | 0.84[AFR][1000 genomes] |
rs1853434 | 0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1853435 | 0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1923954 | 0.88[AFR][1000 genomes] |
rs1923957 | 0.84[AFR][1000 genomes] |
rs2760541 | 0.90[AFR][1000 genomes] |
rs2760542 | 0.90[AFR][1000 genomes] |
rs2760548 | 0.90[AFR][1000 genomes] |
rs2760551 | 0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2760552 | 0.90[AFR][1000 genomes] |
rs2760553 | 0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2760554 | 0.91[AFR][1000 genomes] |
rs2760555 | 0.87[AFR][1000 genomes] |
rs2788927 | 0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2788930 | 0.91[AFR][1000 genomes] |
rs6080133 | 0.84[AFR][1000 genomes] |
rs7273081 | 0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs73901418 | 0.87[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs912183 | 0.90[AFR][1000 genomes] |
rs927560 | 0.90[AFR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1059778 | chr20:15999519-16165895 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv544207 | chr20:15999519-16165895 | Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:16104400-16121600 | Weak transcription | Primary B cells from cord blood | blood |