Variant report
Variant | rs4723914 |
---|---|
Chromosome Location | chr7:39935689-39935690 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:8)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:8 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:39934240..39937212-chr7:39987156..39990695,5 | MCF-7 | breast: | |
2 | chr7:39932180..39934119-chr7:39934393..39936758,2 | MCF-7 | breast: | |
3 | chr7:39662538..39665289-chr7:39934013..39936040,2 | K562 | blood: | |
4 | chr7:39933698..39935841-chr7:40172009..40174486,2 | MCF-7 | breast: | |
5 | chr7:39932888..39935926-chr7:39987671..39991292,5 | MCF-7 | breast: | |
6 | chr7:39934810..39937643-chr7:39987808..39990500,2 | K562 | blood: | |
7 | chr7:39925804..39928770-chr7:39934507..39936424,2 | K562 | blood: | |
8 | chr7:39934010..39936310-chr7:39987808..39989967,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000168303 | Chromatin interaction |
ENSG00000065883 | Chromatin interaction |
ENSG00000006451 | Chromatin interaction |
ENSG00000242855 | Chromatin interaction |
ENSG00000259826 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10225311 | 0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10270355 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11760665 | 0.95[EUR][1000 genomes] |
rs11973720 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11975808 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11983868 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12701774 | 0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12701776 | 0.97[EUR][1000 genomes] |
rs12701777 | 0.95[EUR][1000 genomes] |
rs12701778 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1523711 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1608500 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes] |
rs2049350 | 0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2049351 | 1.00[CEU][hapmap];0.90[EUR][1000 genomes] |
rs2091092 | 0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2329608 | 0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2329609 | 0.99[ASN][1000 genomes] |
rs2329610 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3966561 | 0.92[ASN][1000 genomes] |
rs4720343 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4723915 | 0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6462952 | 0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6462953 | 0.90[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6947780 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6949575 | 0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6957432 | 0.99[ASN][1000 genomes] |
rs6969026 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6979770 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs72589780 | 0.99[ASN][1000 genomes] |
rs72589783 | 0.92[ASN][1000 genomes] |
rs7777774 | 0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7787480 | 0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7789497 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9638946 | 0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv427777 | chr7:39726513-39936904 | Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
2 | nsv887973 | chr7:39772654-40110720 | Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 58 gene(s) | inside rSNPs | diseases |
3 | nsv887974 | chr7:39827400-39956829 | Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv887975 | chr7:39858378-40124137 | Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 49 gene(s) | inside rSNPs | diseases |
5 | nsv887976 | chr7:39874986-40018693 | Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 47 gene(s) | inside rSNPs | diseases |
6 | nsv887977 | chr7:39885541-40018693 | ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 46 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:39934200-39936000 | Enhancers | Breast Myoepithelial Primary Cells | Breast |