Variant report
| Variant | rs2704213 |
|---|---|
| Chromosome Location | chr15:58405808-58405809 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:5 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr15:58402876..58406319-chr15:58411755..58414973,3 | K562 | blood: | |
| 2 | chr15:58404558..58406881-chr15:58443582..58445148,2 | K562 | blood: | |
| 3 | chr15:58389052..58391594-chr15:58404567..58406553,2 | K562 | blood: | |
| 4 | chr15:58360768..58363074-chr15:58403366..58406297,2 | K562 | blood: | |
| 5 | chr15:58402749..58406127-chr15:58406949..58409453,4 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000259379 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:15)
| rs_ID | r2[population] |
|---|---|
| rs1829135 | 0.89[EUR][1000 genomes] |
| rs2063902 | 1.00[ASN][1000 genomes] |
| rs2453277 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2464465 | 0.87[EUR][1000 genomes] |
| rs2464470 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2642615 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2642620 | 0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2642654 | 0.95[ASN][1000 genomes] |
| rs2642656 | 1.00[ASN][1000 genomes] |
| rs2704210 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2704211 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs2704212 | 1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs2704230 | 0.92[EUR][1000 genomes] |
| rs7183406 | 0.95[ASN][1000 genomes] |
| rs8027250 | 0.95[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1038667 | chr15:57933076-58481870 | Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
| 2 | nsv542400 | chr15:57933076-58481870 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
| 3 | nsv904263 | chr15:58340072-58437346 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| 4 | nsv569596 | chr15:58355798-58408763 | Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
| 5 | nsv1047246 | chr15:58375607-58707158 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr15:58405400-58408400 | Enhancers | K562 | blood |
