Variant report
Variant | rs12329855 |
---|---|
Chromosome Location | chr21:47204727-47204728 |
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 | chr21:47204063..47206978-chr21:47208624..47210264,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12329841 | 0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs12482648 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12482853 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2094888 | 0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2183595 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2183596 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2838989 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2838990 | 0.80[ASN][1000 genomes] |
rs2838991 | 0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2838992 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2838993 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2838994 | 0.81[EUR][1000 genomes] |
rs2838995 | 0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2838996 | 0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2838997 | 0.83[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs2838998 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2838999 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2839000 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2839002 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2839003 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2839004 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs2839005 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2839009 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs28583990 | 0.80[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs3367 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4818798 | 0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4818801 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs4819151 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs4819152 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs55707606 | 0.82[ASN][1000 genomes] |
rs55780126 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs55875620 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs56012600 | 0.80[ASN][1000 genomes] |
rs56036552 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs56256701 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs56323347 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs56347571 | 0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs56378934 | 0.82[ASN][1000 genomes] |
rs58952758 | 0.88[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs59398815 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs59785950 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs60604183 | 0.80[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs61100346 | 0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs62213555 | 0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs62214592 | 0.88[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs62214596 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs62214597 | 0.88[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs62214599 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs62214604 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs66552772 | 0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs66991496 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7276632 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs8127369 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs8127809 | 0.80[ASN][1000 genomes] |
rs8128722 | 0.83[ASN][1000 genomes] |
rs914241 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9637205 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs9637206 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs9647230 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9974491 | 0.80[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9977309 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs9977908 | 0.80[EUR][1000 genomes] |
rs9978078 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9978740 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531546 | chr21:46504151-47411772 | Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 93 gene(s) | inside rSNPs | diseases |
2 | nsv1058665 | chr21:46719445-47634282 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 91 gene(s) | inside rSNPs | diseases |
3 | nsv544486 | chr21:46719445-47634282 | Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 91 gene(s) | inside rSNPs | diseases |
4 | nsv1059230 | chr21:46956877-47907990 | Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 94 gene(s) | inside rSNPs | n/a |
5 | nsv544491 | chr21:46956877-47907990 | Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 94 gene(s) | inside rSNPs | n/a |
6 | nsv1058472 | chr21:47027823-47797326 | Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | n/a |
7 | nsv544492 | chr21:47027823-47797326 | Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | n/a |
8 | nsv428043 | chr21:47179244-47471971 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | n/a |
9 | nsv1065959 | chr21:47188878-48091343 | Bivalent Enhancer Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 102 gene(s) | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:47188800-47208000 | Weak transcription | NHDF-Ad | bronchial |
2 | chr21:47197400-47214200 | Weak transcription | Primary T cells from cord blood | blood |
3 | chr21:47199200-47212800 | Weak transcription | Fetal Thymus | thymus |
4 | chr21:47199400-47206600 | Weak transcription | Thymus | Thymus |
5 | chr21:47199400-47217200 | Weak transcription | Spleen | Spleen |