Variant report
Variant | rs66947818 |
---|---|
Chromosome Location | chr5:50323230-50323231 |
allele | C/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)
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(count:3 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000100083 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10805506 | 0.82[ASN][1000 genomes] |
rs10940613 | 0.87[ASN][1000 genomes] |
rs12657116 | 0.83[ASN][1000 genomes] |
rs12659587 | 0.87[ASN][1000 genomes] |
rs13175573 | 0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13177246 | 0.87[ASN][1000 genomes] |
rs1423227 | 0.85[ASN][1000 genomes] |
rs1545350 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2289879 | 0.87[ASN][1000 genomes] |
rs2289880 | 0.87[ASN][1000 genomes] |
rs250216 | 0.87[ASN][1000 genomes] |
rs35192063 | 0.87[ASN][1000 genomes] |
rs35477295 | 0.87[ASN][1000 genomes] |
rs35894462 | 0.87[ASN][1000 genomes] |
rs4866019 | 0.87[ASN][1000 genomes] |
rs4866020 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1034445 | chr5:49986171-50492609 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv830286 | chr5:50165805-50374600 | Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv1018897 | chr5:50284474-50344007 | Enhancers Active TSS Weak transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv537762 | chr5:50284474-50344007 | Enhancers Weak transcription Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |