Variant report
| Variant | rs17158234 |
|---|---|
| Chromosome Location | chr7:103658843-103658844 |
| allele | C/T |
| Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:4 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr7:103648042..103650999-chr7:103656412..103659096,2 | K562 | blood: | |
| 2 | chr7:103657443..103659638-chr7:103669864..103671987,2 | K562 | blood: | |
| 3 | chr7:103628980..103630877-chr7:103656452..103658891,2 | K562 | blood: | |
| 4 | chr7:103658138..103659805-chr7:103669387..103671987,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000189056 | Chromatin interaction |
| rs_ID | r2[population] |
|---|---|
| rs10246267 | 0.82[CEU][hapmap] |
| rs10260517 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs10275334 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs17158084 | 1.00[CEU][hapmap];0.97[EUR][1000 genomes] |
| rs17158117 | 1.00[EUR][1000 genomes] |
| rs28375592 | 1.00[EUR][1000 genomes] |
| rs28542542 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6465954 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6465958 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6964023 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs6970904 | 1.00[CEU][hapmap] |
| rs9986801 | 1.00[CEU][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv888924 | chr7:103637906-103706936 | Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
| No data |





