Variant report
Variant | rs927920 |
---|---|
Chromosome Location | chr20:15400731-15400732 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr20:15400360..15402078-chr20:15403721..15405394,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12481556 | 0.81[YRI][hapmap] |
rs1326670 | 0.85[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1468888 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes] |
rs2104589 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2208137 | 0.85[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs380512 | 0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs394042 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs426845 | 0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs453612 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs4814370 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4814371 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs4814376 | 0.85[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs6034182 | 0.97[YRI][hapmap];0.85[AFR][1000 genomes] |
rs6034183 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6034185 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs6034186 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs6034188 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6034191 | 0.85[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes] |
rs6034194 | 0.96[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6043268 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6043269 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6043270 | 0.80[YRI][hapmap] |
rs6043282 | 0.85[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6043283 | 0.82[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.88[ASN][1000 genomes] |
rs6043287 | 0.85[CEU][hapmap];0.81[CHB][hapmap];0.84[ASN][1000 genomes] |
rs6079821 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6079828 | 0.82[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6079833 | 0.83[CEU][hapmap];0.84[ASN][1000 genomes] |
rs6110606 | 0.81[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes] |
rs727245 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs727246 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs727247 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs932822 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1062252 | chr20:14964258-15547739 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv544206 | chr20:14964258-15547739 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | 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 |
4 | nsv833927 | chr20:15362602-15520185 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:15399000-15401000 | Enhancers | Colon Smooth Muscle | Colon |