Variant report
Variant | rs62339769 |
---|---|
Chromosome Location | chr4:160701772-160701773 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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Variant related genes | Relation type |
---|---|
ENSG00000250488 | TF binding region |
rs_ID | r2[population] |
---|---|
rs1502746 | 0.92[ASN][1000 genomes] |
rs1502747 | 0.92[ASN][1000 genomes] |
rs17038749 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs17038762 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs17038893 | 1.00[AMR][1000 genomes] |
rs62332987 | 1.00[AMR][1000 genomes] |
rs62332988 | 1.00[AMR][1000 genomes] |
rs62332990 | 1.00[AMR][1000 genomes] |
rs62332991 | 1.00[AMR][1000 genomes] |
rs62332992 | 1.00[AMR][1000 genomes] |
rs62333019 | 1.00[AMR][1000 genomes] |
rs62333022 | 1.00[AMR][1000 genomes] |
rs62333028 | 1.00[AMR][1000 genomes] |
rs62333029 | 1.00[AMR][1000 genomes] |
rs62335365 | 0.83[AMR][1000 genomes] |
rs62335366 | 0.83[AMR][1000 genomes] |
rs62338532 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62338533 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62338534 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62338537 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7669796 | 0.89[ASN][1000 genomes] |
rs7684510 | 0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1015469 | chr4:160389277-160841619 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv537316 | chr4:160389277-160841619 | Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv880358 | chr4:160694415-161575183 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |