Variant report
Variant | rs60723945 |
---|---|
Chromosome Location | chr3:24106714-24106715 |
allele | A/G |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:23956560..23959244-chr3:24104963..24107310,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000174748 | Chromatin interaction |
ENSG00000197885 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11920383 | 1.00[EUR][1000 genomes] |
rs11924501 | 1.00[EUR][1000 genomes] |
rs11924778 | 1.00[EUR][1000 genomes] |
rs17014086 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17014087 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1900996 | 1.00[EUR][1000 genomes] |
rs1900997 | 1.00[EUR][1000 genomes] |
rs2089850 | 1.00[AMR][1000 genomes] |
rs4377442 | 1.00[EUR][1000 genomes] |
rs4467390 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4510334 | 1.00[AMR][1000 genomes] |
rs56229046 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs56259756 | 1.00[EUR][1000 genomes] |
rs56711878 | 1.00[EUR][1000 genomes] |
rs58538965 | 1.00[EUR][1000 genomes] |
rs58996984 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59740610 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60523116 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61543192 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6550843 | 1.00[EUR][1000 genomes] |
rs73134545 | 1.00[EUR][1000 genomes] |
rs73134552 | 1.00[EUR][1000 genomes] |
rs73134553 | 1.00[EUR][1000 genomes] |
rs73134559 | 1.00[EUR][1000 genomes] |
rs73822649 | 1.00[AMR][1000 genomes] |
rs73822653 | 1.00[AMR][1000 genomes] |
rs73822689 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73822697 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73822701 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73825905 | 1.00[AMR][1000 genomes] |
rs73825908 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73825909 | 1.00[AMR][1000 genomes] |
rs73825915 | 1.00[EUR][1000 genomes] |
rs73825916 | 1.00[EUR][1000 genomes] |
rs73825917 | 1.00[EUR][1000 genomes] |
rs73825918 | 1.00[EUR][1000 genomes] |
rs73825919 | 1.00[EUR][1000 genomes] |
rs73825920 | 1.00[EUR][1000 genomes] |
rs7637983 | 1.00[EUR][1000 genomes] |
rs873451 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533980 | chr3:23445901-24311972 | ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 64 gene(s) | inside rSNPs | diseases |
2 | nsv834638 | chr3:23963860-24117191 | Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
3 | nsv834639 | chr3:24037113-24233925 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
4 | nsv1004037 | chr3:24064777-24143719 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:24101400-24119200 | Weak transcription | Aorta | Aorta |
2 | chr3:24102200-24109200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr3:24102200-24110400 | Weak transcription | Colon Smooth Muscle | Colon |
4 | chr3:24102400-24106800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
5 | chr3:24105000-24110200 | Weak transcription | Rectal Smooth Muscle | rectum |