Variant report
Variant | rs73578237 |
---|---|
Chromosome Location | chr6:147160421-147160422 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
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(count:1 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-SHPRH-2 | chr6:147160003-147163945 | NONHSAT115432 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000233452 | Chromatin interaction |
ENSG00000164506 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17076347 | 0.82[AFR][1000 genomes] |
rs17076349 | 0.83[AFR][1000 genomes] |
rs17076351 | 0.84[AFR][1000 genomes] |
rs4343936 | 0.83[AFR][1000 genomes] |
rs4404785 | 0.83[AFR][1000 genomes] |
rs4538736 | 0.83[AFR][1000 genomes] |
rs73576271 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73576284 | 0.83[AFR][1000 genomes] |
rs73576287 | 0.83[AFR][1000 genomes] |
rs73576288 | 0.83[AFR][1000 genomes] |
rs73576296 | 0.81[AFR][1000 genomes] |
rs73576301 | 0.96[AFR][1000 genomes] |
rs73576302 | 0.82[AFR][1000 genomes] |
rs73578203 | 0.82[AFR][1000 genomes] |
rs73578204 | 0.82[AFR][1000 genomes] |
rs73578205 | 0.81[AFR][1000 genomes] |
rs73578229 | 0.84[AFR][1000 genomes] |
rs73578284 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7451402 | 0.83[AFR][1000 genomes] |
rs7453957 | 0.83[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830838 | chr6:147090745-147274669 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
2 | esv2451265 | chr6:147159682-147161265 | Enhancers Weak transcription | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:147150200-147162200 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |