Variant report
Variant | rs553592 |
---|---|
Chromosome Location | chr6:118187976-118187977 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs13200447 | 0.84[EUR][1000 genomes] |
rs17334264 | 0.84[EUR][1000 genomes] |
rs2476202 | 0.92[EUR][1000 genomes] |
rs2760227 | 0.88[EUR][1000 genomes] |
rs2760230 | 0.87[EUR][1000 genomes] |
rs2760236 | 0.92[EUR][1000 genomes] |
rs2760237 | 0.92[EUR][1000 genomes] |
rs2760238 | 0.92[EUR][1000 genomes] |
rs2760248 | 0.88[EUR][1000 genomes] |
rs2788994 | 0.88[EUR][1000 genomes] |
rs2788995 | 1.00[EUR][1000 genomes] |
rs2788997 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2788998 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35106048 | 0.84[EUR][1000 genomes] |
rs474078 | 0.91[AFR][1000 genomes] |
rs478718 | 0.93[AFR][1000 genomes] |
rs520888 | 0.91[AFR][1000 genomes] |
rs555789 | 0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6905222 | 0.84[EUR][1000 genomes] |
rs6942237 | 0.91[EUR][1000 genomes] |
rs71570870 | 0.84[EUR][1000 genomes] |
rs7745854 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7765524 | 0.87[EUR][1000 genomes] |
rs9654611 | 0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532050 | chr6:117528154-118203005 | ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
2 | nsv830786 | chr6:118026955-118201660 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv530526 | chr6:118027339-118718476 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:118187600-118188000 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |