Variant report
Variant | rs6984001 |
---|---|
Chromosome Location | chr8:95604669-95604670 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:180)
- CpG islands (count:0)
- Chromatin interactive region (count:6)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
(count:6 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:95604279..95604876-chr8:95624972..95625755,2 | MCF-7 | breast: | |
2 | chr8:95604280..95605218-chr8:95654234..95655141,4 | MCF-7 | breast: | |
3 | chr8:95603957..95608238-chr8:95651708..95655027,4 | MCF-7 | breast: | |
4 | chr8:95603445..95604962-chr8:95650191..95651732,2 | MCF-7 | breast: | |
5 | chr8:95604274..95605200-chr8:95725698..95726286,2 | MCF-7 | breast: | |
6 | chr8:95604246..95605617-chr8:95725348..95726635,8 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000254283 | TF binding region |
ENSG00000261437 | Chromatin interaction |
ENSG00000104413 | Chromatin interaction |
ENSG00000199701 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs3133614 | 0.80[CEU][hapmap] |
rs6987063 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs73261380 | 0.96[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs73261386 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1017301 | chr8:95273503-96248352 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 87 gene(s) | inside rSNPs | diseases |
2 | nsv539680 | chr8:95273503-96248352 | Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 87 gene(s) | inside rSNPs | diseases |
3 | nsv532338 | chr8:95296118-95971825 | Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 61 gene(s) | inside rSNPs | diseases |
4 | nsv429928 | chr8:95488800-95672033 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
5 | nsv429929 | chr8:95564533-95676894 | Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers 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 | 23 gene(s) | inside rSNPs | diseases |
6 | nsv520435 | chr8:95598598-95608367 | Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | esv3350182 | chr8:95601526-95604924 | Inactive region | TF binding regionChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
8 | esv3422133 | chr8:95602201-95604749 | Inactive region | TF binding regionChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |