Variant report
Variant | rs34672734 |
---|---|
Chromosome Location | chr8:117805281-117805282 |
allele | A/G |
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 | chr8:117778464..117780161-chr8:117803069..117805763,2 | MCF-7 | breast: | |
2 | chr8:117804606..117806220-chr8:117812796..117814658,2 | K562 | blood: | |
3 | chr8:117804720..117807505-chr8:117812796..117815488,2 | K562 | blood: | |
4 | chr8:117801485..117803736-chr8:117805253..117808179,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000147679 | Chromatin interaction |
ENSG00000147677 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10095889 | 0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10104144 | 0.82[ASN][1000 genomes] |
rs10283122 | 0.83[ASN][1000 genomes] |
rs10283129 | 0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10808485 | 0.82[ASN][1000 genomes] |
rs11783824 | 0.89[ASN][1000 genomes] |
rs12548402 | 0.83[ASN][1000 genomes] |
rs12675074 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12675093 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13250873 | 0.90[ASN][1000 genomes] |
rs1374299 | 0.91[ASN][1000 genomes] |
rs17664079 | 0.84[ASN][1000 genomes] |
rs1867841 | 0.92[ASN][1000 genomes] |
rs2121339 | 0.85[ASN][1000 genomes] |
rs34701891 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs35682273 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4145242 | 0.82[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4372028 | 0.80[ASN][1000 genomes] |
rs4464999 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4514005 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4876365 | 0.91[ASN][1000 genomes] |
rs4876679 | 0.89[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4876680 | 0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62510194 | 0.85[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs6469660 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6988190 | 0.86[ASN][1000 genomes] |
rs6990665 | 0.91[ASN][1000 genomes] |
rs6992589 | 0.87[ASN][1000 genomes] |
rs7006087 | 0.90[ASN][1000 genomes] |
rs7013007 | 0.88[ASN][1000 genomes] |
rs7014156 | 0.91[ASN][1000 genomes] |
rs7814084 | 0.85[ASN][1000 genomes] |
rs7817878 | 0.92[ASN][1000 genomes] |
rs7828774 | 0.91[ASN][1000 genomes] |
rs7836226 | 0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530386 | chr8:117509968-118391406 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
2 | nsv831434 | chr8:117784467-117977825 | Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
3 | nsv1027259 | chr8:117790928-117842055 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
4 | nsv1034015 | chr8:117790928-117843979 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:117780400-117830200 | Weak transcription | Aorta | Aorta |
2 | chr8:117782000-117814000 | Weak transcription | Ovary | ovary |