Variant report
| Variant | rs73424200 |
|---|---|
| Chromosome Location | chr15:58403991-58403992 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:12)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:12 , 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 | chr15:58213469..58215325-chr15:58403221..58404811,2 | K562 | blood: | |
| 3 | chr15:58402733..58404852-chr15:58471216..58473457,2 | K562 | blood: | |
| 4 | chr15:58402721..58405438-chr15:58406173..58409890,4 | K562 | blood: | |
| 5 | chr15:58389670..58391517-chr15:58401775..58404180,2 | K562 | blood: | |
| 6 | chr15:58360768..58363074-chr15:58403366..58406297,2 | K562 | blood: | |
| 7 | chr15:58402611..58405043-chr15:58470858..58473947,6 | K562 | blood: | |
| 8 | chr15:58356241..58358717-chr15:58403285..58405338,4 | K562 | blood: | |
| 9 | chr15:58370654..58372424-chr15:58402743..58405731,2 | K562 | blood: | |
| 10 | chr15:58354852..58359954-chr15:58398987..58405153,11 | K562 | blood: | |
| 11 | chr15:58402749..58406127-chr15:58406949..58409453,4 | K562 | blood: | |
| 12 | chr15:58401521..58404295-chr15:58452218..58454934,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000128918 | Chromatin interaction |
| ENSG00000259285 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:14)
| rs_ID | r2[population] |
|---|---|
| rs16939728 | 1.00[AMR][1000 genomes] |
| rs28495054 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs28624780 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs2899615 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs35376151 | 1.00[AMR][1000 genomes] |
| rs59848816 | 1.00[AMR][1000 genomes] |
| rs61096848 | 1.00[AMR][1000 genomes] |
| rs73424132 | 1.00[AMR][1000 genomes] |
| rs73424136 | 1.00[AMR][1000 genomes] |
| rs73424158 | 1.00[AMR][1000 genomes] |
| rs73424185 | 1.00[AMR][1000 genomes] |
| rs73424190 | 1.00[AMR][1000 genomes] |
| rs73424201 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs73426106 | 0.96[AFR][1000 genomes];1.00[AMR][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 | chr15:58402800-58404600 | Flanking Active TSS | K562 | blood |
| 2 | chr15:58403800-58404000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
