Variant report
Variant | rs58242629 |
---|---|
Chromosome Location | chr2:100995027-100995028 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:100935841..100941857-chr2:100994239..100999137,10 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000170500 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17023897 | 1.00[EUR][1000 genomes] |
rs17023990 | 0.89[EUR][1000 genomes] |
rs17024021 | 0.89[EUR][1000 genomes] |
rs17024048 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17024150 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17024185 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17024216 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17353694 | 1.00[EUR][1000 genomes] |
rs28827632 | 1.00[EUR][1000 genomes] |
rs3948255 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57669367 | 1.00[EUR][1000 genomes] |
rs57710676 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58420862 | 1.00[EUR][1000 genomes] |
rs58658810 | 1.00[EUR][1000 genomes] |
rs59727890 | 1.00[EUR][1000 genomes] |
rs60078624 | 0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61057466 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61070099 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6732784 | 0.89[EUR][1000 genomes] |
rs6743347 | 1.00[EUR][1000 genomes] |
rs72964116 | 0.89[EUR][1000 genomes] |
rs7582424 | 0.89[EUR][1000 genomes] |
rs7605818 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1007777 | chr2:100816913-101308914 | Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
2 | nsv535844 | chr2:100816913-101308914 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
3 | nsv582531 | chr2:100908508-101207639 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
4 | nsv874701 | chr2:100976139-101023261 | Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:100993200-101017800 | Weak transcription | Primary monocytes fromperipheralblood | blood |