Variant report
Variant | rs1562785 |
---|---|
Chromosome Location | chr8:20562331-20562332 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:8)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:8 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CTCF | chr8:20562270-20562401 | MCF-7 | breast: | n/a | n/a |
2 | CTCF | chr8:20562275-20562403 | MCF-7 | breast: | n/a | n/a |
3 | CTCF | chr8:20562273-20562405 | MCF-7 | breast: | n/a | n/a |
4 | CTCF | chr8:20562274-20562369 | MCF-7 | breast: | n/a | n/a |
5 | CTCF | chr8:20562277-20562393 | MCF-7 | breast: | n/a | n/a |
6 | CTCF | chr8:20562289-20562358 | K562 | blood: | n/a | n/a |
7 | CTCF | chr8:20562322-20562363 | GM12891 | blood: | n/a | n/a |
8 | SPI1 | chr8:20562125-20562463 | HL-60 | blood: | n/a | chr8:20562255-20562264 chr8:20562188-20562195 |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000253300 | TF binding region |
rs_ID | r2[population] |
---|---|
rs17421308 | 0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2597381 | 0.89[ASN][1000 genomes] |
rs2597383 | 0.84[ASN][1000 genomes] |
rs2597384 | 0.80[ASN][1000 genomes] |
rs2597392 | 0.91[CHB][hapmap];0.83[JPT][hapmap];0.98[ASN][1000 genomes] |
rs2597393 | 1.00[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes] |
rs2597405 | 0.83[ASN][1000 genomes] |
rs2597406 | 0.84[ASN][1000 genomes] |
rs2597409 | 0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2616204 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2616233 | 0.83[ASN][1000 genomes] |
rs2616236 | 0.84[ASN][1000 genomes] |
rs2616239 | 0.85[ASN][1000 genomes] |
rs2616250 | 0.93[ASN][1000 genomes] |
rs2616252 | 0.88[ASN][1000 genomes] |
rs2616255 | 0.86[ASN][1000 genomes] |
rs2616256 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4922229 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1033511 | chr8:19751299-20625091 | Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
2 | nsv530877 | chr8:19873053-20593254 | Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
3 | nsv1027535 | chr8:20506377-20613664 | Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1032450 | chr8:20514995-21033577 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
5 | nsv539524 | chr8:20514995-21033577 | Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
6 | esv2761417 | chr8:20523767-20669443 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:20562000-20563000 | Weak transcription | Brain Germinal Matrix | brain |