Variant report
| Variant | rs1977293 |
|---|---|
| Chromosome Location | chr10:50592819-50592820 |
| allele | C/T |
| 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 | chr10:50589316..50590909-chr10:50591054..50594050,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
| rs_ID | r2[population] |
|---|---|
| rs10732632 | 0.86[EUR][1000 genomes] |
| rs10745260 | 0.86[EUR][1000 genomes] |
| rs1570645 | 0.93[YRI][hapmap];0.99[AFR][1000 genomes];0.93[AMR][1000 genomes] |
| rs17009940 | 1.00[EUR][1000 genomes] |
| rs17009941 | 1.00[EUR][1000 genomes] |
| rs17009956 | 1.00[EUR][1000 genomes] |
| rs17009957 | 1.00[EUR][1000 genomes] |
| rs17009961 | 1.00[EUR][1000 genomes] |
| rs17010002 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs2889781 | 1.00[EUR][1000 genomes] |
| rs2889783 | 1.00[EUR][1000 genomes] |
| rs4562729 | 1.00[EUR][1000 genomes] |
| rs58651064 | 1.00[EUR][1000 genomes] |
| rs58733378 | 1.00[EUR][1000 genomes] |
| rs59096752 | 1.00[EUR][1000 genomes] |
| rs59572955 | 1.00[EUR][1000 genomes] |
| rs59959035 | 1.00[EUR][1000 genomes] |
| rs60811583 | 1.00[EUR][1000 genomes] |
| rs61296942 | 0.86[EUR][1000 genomes] |
| rs7900263 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7915692 | 0.80[YRI][hapmap] |
| rs7916121 | 0.83[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 | nsv895375 | chr10:50306386-51028871 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
| 2 | nsv534410 | chr10:50317458-50826916 | Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
| 3 | nsv895377 | chr10:50588990-50678212 | ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:50591600-50594800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |





