Variant report
Variant | rs1006805 |
---|---|
Chromosome Location | chr16:72504919-72504920 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:3 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs1001493 | 0.80[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs10468266 | 0.90[EUR][1000 genomes] |
rs10492821 | 0.81[EUR][1000 genomes] |
rs11641842 | 0.80[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs11860023 | 0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11862324 | 0.95[AFR][1000 genomes] |
rs12051542 | 0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12325146 | 0.91[EUR][1000 genomes] |
rs12325151 | 0.91[EUR][1000 genomes] |
rs12445443 | 0.97[EUR][1000 genomes] |
rs12596611 | 0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12598598 | 0.94[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs12599375 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12708933 | 1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap];0.88[EUR][1000 genomes] |
rs13333122 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs13335806 | 0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1429072 | 0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1560278 | 0.94[EUR][1000 genomes] |
rs16970900 | 0.92[AFR][1000 genomes] |
rs16970908 | 0.83[AFR][1000 genomes] |
rs16971030 | 0.90[EUR][1000 genomes] |
rs16971035 | 0.91[EUR][1000 genomes] |
rs16971036 | 0.91[EUR][1000 genomes] |
rs16971037 | 0.89[EUR][1000 genomes] |
rs16971050 | 0.91[EUR][1000 genomes] |
rs16971112 | 1.00[CEU][hapmap];0.85[EUR][1000 genomes] |
rs16971114 | 0.81[EUR][1000 genomes] |
rs17287903 | 0.86[EUR][1000 genomes] |
rs17359949 | 0.86[EUR][1000 genomes] |
rs17609544 | 0.91[EUR][1000 genomes] |
rs17609577 | 0.91[EUR][1000 genomes] |
rs17609787 | 0.94[EUR][1000 genomes] |
rs17609808 | 0.94[EUR][1000 genomes] |
rs17677484 | 0.94[EUR][1000 genomes] |
rs17677616 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs17677890 | 0.94[EUR][1000 genomes] |
rs17841357 | 0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1864229 | 0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1864231 | 0.84[AFR][1000 genomes] |
rs1991530 | 0.86[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs2079161 | 0.92[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs2158265 | 0.90[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs2158266 | 0.83[AFR][1000 genomes];0.84[AMR][1000 genomes] |
rs2158268 | 0.80[ASN][1000 genomes] |
rs2163068 | 0.90[EUR][1000 genomes] |
rs2358801 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs28677977 | 0.89[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs2905697 | 0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2905699 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2914774 | 0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2914777 | 0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2914779 | 0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2967232 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2967233 | 0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2967234 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2967240 | 0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs35005335 | 0.81[EUR][1000 genomes] |
rs4410082 | 0.86[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs4788473 | 0.94[EUR][1000 genomes] |
rs4788646 | 0.83[EUR][1000 genomes] |
rs55766519 | 0.91[EUR][1000 genomes] |
rs55808336 | 0.94[EUR][1000 genomes] |
rs56152199 | 0.90[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs56323671 | 0.87[EUR][1000 genomes] |
rs56347149 | 0.90[EUR][1000 genomes] |
rs56348767 | 0.92[EUR][1000 genomes] |
rs56389222 | 0.92[EUR][1000 genomes] |
rs56404261 | 0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs57220817 | 0.94[EUR][1000 genomes] |
rs58549165 | 0.94[EUR][1000 genomes] |
rs58745414 | 0.94[EUR][1000 genomes] |
rs58770834 | 0.90[EUR][1000 genomes] |
rs58860566 | 0.91[EUR][1000 genomes] |
rs60502114 | 0.91[EUR][1000 genomes] |
rs61475520 | 0.91[EUR][1000 genomes] |
rs62051139 | 0.90[AFR][1000 genomes] |
rs62051486 | 0.86[EUR][1000 genomes] |
rs62051488 | 0.86[EUR][1000 genomes] |
rs62051497 | 0.80[EUR][1000 genomes] |
rs62052877 | 0.89[EUR][1000 genomes] |
rs62052878 | 0.90[EUR][1000 genomes] |
rs62052879 | 0.91[EUR][1000 genomes] |
rs62052880 | 0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs62052881 | 0.91[EUR][1000 genomes] |
rs62052888 | 0.91[EUR][1000 genomes] |
rs62052890 | 0.94[EUR][1000 genomes] |
rs62052891 | 0.94[EUR][1000 genomes] |
rs62052894 | 0.84[EUR][1000 genomes] |
rs62052895 | 0.94[EUR][1000 genomes] |
rs62052909 | 0.94[EUR][1000 genomes] |
rs62052911 | 0.94[EUR][1000 genomes] |
rs62052915 | 0.89[EUR][1000 genomes] |
rs62052920 | 0.91[EUR][1000 genomes] |
rs62052921 | 0.91[EUR][1000 genomes] |
rs62052923 | 0.84[EUR][1000 genomes] |
rs62052927 | 0.90[EUR][1000 genomes] |
rs62052954 | 0.90[EUR][1000 genomes] |
rs62054469 | 0.86[EUR][1000 genomes] |
rs62054470 | 0.86[EUR][1000 genomes] |
rs7188640 | 0.93[EUR][1000 genomes] |
rs7189331 | 0.94[EUR][1000 genomes] |
rs7192221 | 0.90[EUR][1000 genomes] |
rs7193177 | 0.94[EUR][1000 genomes] |
rs7194470 | 0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7194533 | 0.92[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs7198233 | 0.90[EUR][1000 genomes] |
rs7198431 | 0.94[EUR][1000 genomes] |
rs7198788 | 0.90[EUR][1000 genomes] |
rs7199970 | 0.90[EUR][1000 genomes] |
rs7205109 | 1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.93[EUR][1000 genomes] |
rs72793252 | 0.89[EUR][1000 genomes] |
rs72793263 | 0.92[EUR][1000 genomes] |
rs72793266 | 0.91[EUR][1000 genomes] |
rs72793271 | 0.91[EUR][1000 genomes] |
rs8046070 | 0.94[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs8046749 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs8047866 | 0.91[AFR][1000 genomes] |
rs8048181 | 0.84[EUR][1000 genomes] |
rs8048832 | 1.00[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes] |
rs8049577 | 0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs8050815 | 0.87[EUR][1000 genomes] |
rs8057278 | 0.97[AFR][1000 genomes];0.82[AMR][1000 genomes] |
rs8059626 | 0.82[EUR][1000 genomes] |
rs8060607 | 0.81[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs8064129 | 0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs806734 | 0.97[YRI][hapmap] |
rs806745 | 0.81[ASN][1000 genomes] |
rs877641 | 0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9302637 | 0.94[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs9630625 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9922217 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9924296 | 0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9925470 | 0.91[EUR][1000 genomes] |
rs9936195 | 0.82[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs999697 | 0.90[EUR][1000 genomes] |
rs999698 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948468 | chr16:71727571-72651914 | Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 89 gene(s) | inside rSNPs | diseases |
2 | nsv1060983 | chr16:72074832-72791629 | Genic enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 58 gene(s) | inside rSNPs | diseases |
3 | nsv1060804 | chr16:72078486-72791629 | Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 58 gene(s) | inside rSNPs | diseases |
4 | nsv534039 | chr16:72287171-72851170 | Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 36 gene(s) | inside rSNPs | diseases |
5 | nsv1063172 | chr16:72342110-72537808 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
6 | nsv542947 | chr16:72342110-72537808 | ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
7 | nsv1067525 | chr16:72342110-72602796 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
8 | nsv542948 | chr16:72342110-72602796 | ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
9 | nsv1057127 | chr16:72375524-72509686 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
10 | nsv542949 | chr16:72375524-72509686 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
11 | nsv1055807 | chr16:72418417-72614308 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
12 | nsv572956 | chr16:72426448-72517014 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
13 | nsv523524 | chr16:72464460-72635674 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
14 | nsv1055142 | chr16:72473520-72627783 | ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
15 | nsv542950 | chr16:72473520-72627783 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
16 | nsv530712 | chr16:72499171-72744114 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:72489600-72508400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr16:72494600-72516800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
3 | chr16:72499200-72505000 | Weak transcription | Primary B cells from cord blood | blood |
4 | chr16:72499800-72508600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
5 | chr16:72503000-72507200 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
6 | chr16:72503000-72507600 | Weak transcription | Muscle Satellite Cultured Cells | -- |
7 | chr16:72503000-72508200 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
8 | chr16:72503600-72505000 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
9 | chr16:72504000-72507800 | Weak transcription | Brain Cingulate Gyrus | brain |
10 | chr16:72504200-72509600 | Weak transcription | Fetal Heart | heart |
11 | chr16:72504400-72505400 | Enhancers | HepG2 | liver |
12 | chr16:72504600-72507200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
13 | chr16:72504800-72508200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |