Variant report
Variant | rs74018836 |
---|---|
Chromosome Location | chr15:58348986-58348987 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr15:58347698..58349287-chr15:58357341..58359219,2 | MCF-7 | breast: | |
2 | chr15:58346910..58349954-chr15:58473390..58475572,3 | K562 | blood: | |
3 | chr15:58330591..58332432-chr15:58347287..58349860,2 | K562 | blood: | |
4 | chr15:58348390..58350453-chr15:58469668..58473033,3 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000128918 | Chromatin interaction |
ENSG00000259285 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs34365924 | 0.83[AFR][1000 genomes] |
rs34527708 | 0.83[AFR][1000 genomes] |
rs35514555 | 0.83[AFR][1000 genomes] |
rs56114312 | 1.00[AMR][1000 genomes] |
rs56787487 | 1.00[AMR][1000 genomes] |
rs57297157 | 1.00[AMR][1000 genomes] |
rs57557175 | 1.00[AMR][1000 genomes] |
rs57882243 | 1.00[AMR][1000 genomes] |
rs59302780 | 1.00[AMR][1000 genomes] |
rs60201017 | 1.00[AMR][1000 genomes] |
rs74016540 | 1.00[AMR][1000 genomes] |
rs74016543 | 1.00[AMR][1000 genomes] |
rs74016574 | 1.00[AMR][1000 genomes] |
rs74016575 | 1.00[AMR][1000 genomes] |
rs74016576 | 1.00[AMR][1000 genomes] |
rs74016578 | 1.00[AMR][1000 genomes] |
rs74016579 | 1.00[AMR][1000 genomes] |
rs74016580 | 1.00[AMR][1000 genomes] |
rs74016581 | 1.00[AMR][1000 genomes] |
rs74016584 | 1.00[AMR][1000 genomes] |
rs74016585 | 1.00[AMR][1000 genomes] |
rs74016586 | 1.00[AMR][1000 genomes] |
rs74016589 | 1.00[AMR][1000 genomes] |
rs74016590 | 1.00[AMR][1000 genomes] |
rs74016591 | 1.00[AMR][1000 genomes] |
rs74018817 | 1.00[AMR][1000 genomes] |
rs74018826 | 1.00[AMR][1000 genomes] |
rs74018834 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74018844 | 1.00[AMR][1000 genomes] |
rs74018846 | 1.00[AMR][1000 genomes] |
rs74018847 | 1.00[AMR][1000 genomes] |
rs74018848 | 1.00[AMR][1000 genomes] |
rs74018850 | 1.00[AMR][1000 genomes] |
rs74018851 | 1.00[AMR][1000 genomes] |
rs74018954 | 1.00[AMR][1000 genomes] |
rs74018956 | 1.00[AMR][1000 genomes] |
rs74018958 | 1.00[AMR][1000 genomes] |
rs8037139 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1038667 | chr15:57933076-58481870 | Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv542400 | chr15:57933076-58481870 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | nsv904262 | chr15:58340072-58355798 | Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv904263 | chr15:58340072-58437346 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
5 | nsv569595 | chr15:58343146-58353335 | Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:58344200-58349000 | Weak transcription | K562 | blood |
2 | chr15:58347200-58350200 | Weak transcription | Fetal Kidney | kidney |