Variant report
Variant | rs9292072 |
---|---|
Chromosome Location | chr5:54065445-54065446 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000178996 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10036257 | 0.82[ASN][1000 genomes] |
rs10036606 | 0.82[ASN][1000 genomes] |
rs10039924 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10042288 | 0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10042394 | 0.82[ASN][1000 genomes] |
rs10042495 | 0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10045175 | 0.82[ASN][1000 genomes] |
rs10045765 | 0.82[ASN][1000 genomes] |
rs10045790 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10050561 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10053168 | 0.85[ASN][1000 genomes] |
rs10057871 | 0.82[ASN][1000 genomes] |
rs10058571 | 0.82[ASN][1000 genomes] |
rs10058862 | 0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10061958 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10066294 | 0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10066622 | 0.82[ASN][1000 genomes] |
rs10068073 | 0.94[ASN][1000 genomes] |
rs10071183 | 0.93[ASN][1000 genomes] |
rs10073662 | 0.93[ASN][1000 genomes] |
rs10073721 | 0.93[ASN][1000 genomes] |
rs10073837 | 0.96[ASN][1000 genomes] |
rs10434559 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10461588 | 0.85[ASN][1000 genomes] |
rs10471923 | 0.82[ASN][1000 genomes] |
rs1073709 | 0.82[ASN][1000 genomes] |
rs10805463 | 0.85[ASN][1000 genomes] |
rs10805469 | 0.81[ASN][1000 genomes] |
rs10940427 | 0.88[EUR][1000 genomes] |
rs10940428 | 0.82[ASN][1000 genomes] |
rs11950757 | 0.96[ASN][1000 genomes] |
rs11959080 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12514244 | 0.82[ASN][1000 genomes] |
rs12515327 | 0.81[ASN][1000 genomes] |
rs12520494 | 0.81[ASN][1000 genomes] |
rs12522199 | 0.82[ASN][1000 genomes] |
rs13155441 | 0.82[ASN][1000 genomes] |
rs13167527 | 0.82[ASN][1000 genomes] |
rs13173669 | 0.82[ASN][1000 genomes] |
rs13180287 | 0.82[ASN][1000 genomes] |
rs13186826 | 0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs16883428 | 0.86[ASN][1000 genomes] |
rs1867685 | 0.81[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs4242044 | 0.93[ASN][1000 genomes] |
rs4242045 | 0.82[ASN][1000 genomes] |
rs4242046 | 0.81[ASN][1000 genomes] |
rs4242047 | 0.81[ASN][1000 genomes] |
rs4282277 | 0.94[ASN][1000 genomes] |
rs4289528 | 0.81[ASN][1000 genomes] |
rs4290968 | 0.85[ASN][1000 genomes] |
rs4292417 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4298212 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4320207 | 0.81[ASN][1000 genomes] |
rs4336310 | 0.85[ASN][1000 genomes] |
rs4356994 | 0.93[ASN][1000 genomes] |
rs4362906 | 0.82[ASN][1000 genomes] |
rs4457032 | 0.85[ASN][1000 genomes] |
rs4498213 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4515247 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4519880 | 0.82[ASN][1000 genomes] |
rs4527555 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4527556 | 0.82[ASN][1000 genomes] |
rs4591702 | 0.82[ASN][1000 genomes] |
rs4610422 | 0.82[ASN][1000 genomes] |
rs4865870 | 0.83[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4865872 | 0.93[ASN][1000 genomes] |
rs4865873 | 0.85[ASN][1000 genomes] |
rs4865874 | 0.85[ASN][1000 genomes] |
rs4865875 | 0.82[ASN][1000 genomes] |
rs4865876 | 0.82[ASN][1000 genomes] |
rs59595173 | 0.94[ASN][1000 genomes] |
rs59664922 | 1.00[ASN][1000 genomes] |
rs60548640 | 0.97[ASN][1000 genomes] |
rs6450247 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6450248 | 1.00[ASN][1000 genomes] |
rs6450251 | 0.82[ASN][1000 genomes] |
rs6450252 | 0.82[ASN][1000 genomes] |
rs6450253 | 0.82[ASN][1000 genomes] |
rs6860729 | 0.94[ASN][1000 genomes] |
rs6863705 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6867867 | 0.93[ASN][1000 genomes] |
rs6892315 | 0.93[ASN][1000 genomes] |
rs6899052 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs73126822 | 1.00[ASN][1000 genomes] |
rs73126828 | 1.00[ASN][1000 genomes] |
rs73126830 | 1.00[ASN][1000 genomes] |
rs7446423 | 0.82[ASN][1000 genomes] |
rs7709225 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7709401 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7726707 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7728303 | 0.82[ASN][1000 genomes] |
rs9292073 | 0.93[ASN][1000 genomes] |
rs9292074 | 0.82[ASN][1000 genomes] |
rs9687636 | 0.82[ASN][1000 genomes] |
rs9968754 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv880717 | chr5:54025701-54106378 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv830300 | chr5:54056300-54257344 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:54060600-54070000 | Weak transcription | Fetal Muscle Leg | muscle |
2 | chr5:54061000-54070400 | Weak transcription | NHLF | lung |
3 | chr5:54061200-54067000 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
4 | chr5:54064200-54067000 | Weak transcription | Primary B cells from peripheral blood | blood |