Variant report
Variant | rs17625922 |
---|---|
Chromosome Location | chr12:59419208-59419209 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10506353 | 0.81[ASN][1000 genomes] |
rs10735877 | 1.00[CHB][hapmap] |
rs11831827 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17121768 | 0.83[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs17536158 | 0.93[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs17537478 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17618789 | 1.00[CHB][hapmap];0.86[JPT][hapmap] |
rs17626131 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17628225 | 0.83[ASN][1000 genomes] |
rs4760146 | 0.85[ASN][1000 genomes] |
rs55670466 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56042852 | 0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs56299412 | 0.83[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs56376361 | 0.83[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs59263143 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs61934327 | 0.83[ASN][1000 genomes] |
rs61934328 | 0.83[ASN][1000 genomes] |
rs61934330 | 0.83[ASN][1000 genomes] |
rs61934332 | 0.81[ASN][1000 genomes] |
rs7134004 | 0.97[ASN][1000 genomes] |
rs767773 | 0.83[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7955499 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs907344 | 0.91[ASN][1000 genomes] |
rs9668093 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs978615 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1043385 | chr12:59149582-59758952 | Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
2 | nsv1067596 | chr12:59167152-59764208 | Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
3 | nsv492251 | chr12:59167152-59764208 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
4 | nsv559048 | chr12:59336737-59440659 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv559049 | chr12:59359937-59436179 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv526485 | chr12:59412802-59422668 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
7 | nsv522058 | chr12:59416727-59422668 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:59408600-59420800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr12:59417600-59430200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr12:59419200-59426400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |