Variant report
Variant | rs2669425 |
---|---|
Chromosome Location | chr8:105395583-105395584 |
allele | C/T |
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)
(count:1 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | RUNX3 | chr8:105395544-105395956 | GM12878 | blood: | n/a | chr8:105395746-105395755 chr8:105395746-105395755 |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
DPYS | TF binding region |
rs_ID | r2[population] |
---|---|
rs1317380 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes] |
rs1317472 | 0.94[CEU][hapmap];0.89[GIH][hapmap];0.87[EUR][1000 genomes] |
rs1325 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes] |
rs1327 | 0.85[EUR][1000 genomes] |
rs13282328 | 0.81[EUR][1000 genomes] |
rs1513025 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes] |
rs1513026 | 0.83[CEU][hapmap];0.87[EUR][1000 genomes] |
rs2246650 | 0.86[GIH][hapmap];0.87[EUR][1000 genomes] |
rs2669423 | 0.87[EUR][1000 genomes] |
rs2853154 | 1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2853155 | 0.94[CEU][hapmap];0.85[EUR][1000 genomes] |
rs2853158 | 0.94[CEU][hapmap];0.89[GIH][hapmap];0.83[EUR][1000 genomes] |
rs3737535 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes] |
rs3793360 | 0.87[EUR][1000 genomes] |
rs3793361 | 0.87[EUR][1000 genomes] |
rs4734793 | 0.83[CEU][hapmap];0.86[EUR][1000 genomes] |
rs58596729 | 0.87[EUR][1000 genomes] |
rs58903502 | 0.87[EUR][1000 genomes] |
rs6989353 | 0.87[EUR][1000 genomes] |
rs6989484 | 0.82[CEU][hapmap];0.87[EUR][1000 genomes] |
rs6989588 | 0.83[CEU][hapmap];0.87[EUR][1000 genomes] |
rs6994791 | 0.83[EUR][1000 genomes] |
rs6994920 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes] |
rs7000266 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes] |
rs7012566 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes] |
rs7012764 | 0.83[CEU][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes] |
rs870789 | 0.94[CEU][hapmap];0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1016087 | chr8:105228670-105934368 | Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv1032775 | chr8:105311364-105409972 | Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1026754 | chr8:105382508-106030916 | Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
4 | nsv539709 | chr8:105382508-106030916 | Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:105390400-105421000 | Strong transcription | Liver | Liver |
2 | chr8:105393400-105395600 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr8:105394800-105395600 | Enhancers | GM12878-XiMat | blood |