Variant report
| Variant | rs73155730 |
|---|---|
| Chromosome Location | chr7:137765802-137765803 |
| allele | G/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:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr7:137745328..137748047-chr7:137765457..137767555,2 | K562 | blood: | |
| 2 | chr7:137759066..137761270-chr7:137763871..137766101,2 | K562 | blood: | |
| 3 | chr7:137758486..137761270-chr7:137763871..137767061,3 | K562 | blood: | |
| 4 | chr7:137761079..137762998-chr7:137763211..137766028,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000122787 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:16)
| rs_ID | r2[population] |
|---|---|
| rs12668157 | 0.97[ASN][1000 genomes] |
| rs12670239 | 0.91[EUR][1000 genomes] |
| rs1601823 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
| rs17169507 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
| rs17543126 | 0.93[EUR][1000 genomes] |
| rs1872928 | 0.97[ASN][1000 genomes] |
| rs3857869 | 0.83[EUR][1000 genomes] |
| rs3902226 | 0.84[EUR][1000 genomes] |
| rs55970557 | 0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs58783780 | 0.80[ASN][1000 genomes] |
| rs73155727 | 0.97[ASN][1000 genomes] |
| rs73155728 | 0.97[ASN][1000 genomes] |
| rs73155736 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs73155744 | 0.93[EUR][1000 genomes] |
| rs73155746 | 0.84[EUR][1000 genomes] |
| rs7812287 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv518070 | chr7:137534627-137808839 | Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
| 2 | nsv831151 | chr7:137711447-137865471 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 14 gene(s) | inside rSNPs | diseases |
| 3 | esv34048 | chr7:137724092-138213119 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 35 gene(s) | inside rSNPs | diseases |
| 4 | nsv437032 | chr7:137753091-137773291 | Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:137765000-137767000 | Enhancers | Liver | Liver |
