Variant report
Variant | rs4788473 |
---|---|
Chromosome Location | chr16:72641882-72641883 |
allele | A/T |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1001493 | 0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1006805 | 0.94[EUR][1000 genomes] |
rs10468266 | 0.89[EUR][1000 genomes] |
rs11641842 | 0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11860023 | 0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs12051542 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12325146 | 0.85[EUR][1000 genomes] |
rs12325151 | 0.85[EUR][1000 genomes] |
rs12445296 | 0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12445443 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12596611 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs12598536 | 0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs12598598 | 0.80[AFR][1000 genomes] |
rs12599375 | 0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12708933 | 0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs13333122 | 0.91[EUR][1000 genomes] |
rs13335806 | 0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1429072 | 0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1560278 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs16971030 | 0.89[EUR][1000 genomes] |
rs16971035 | 0.87[EUR][1000 genomes] |
rs16971036 | 0.87[EUR][1000 genomes] |
rs16971037 | 0.85[EUR][1000 genomes] |
rs16971050 | 0.87[EUR][1000 genomes] |
rs16971112 | 0.89[EUR][1000 genomes] |
rs16971114 | 0.83[EUR][1000 genomes] |
rs17287903 | 0.92[EUR][1000 genomes] |
rs17359949 | 0.92[EUR][1000 genomes] |
rs17609544 | 0.85[EUR][1000 genomes] |
rs17609577 | 0.85[EUR][1000 genomes] |
rs17609787 | 0.87[EUR][1000 genomes] |
rs17609808 | 0.87[EUR][1000 genomes] |
rs17677484 | 0.87[EUR][1000 genomes] |
rs17677616 | 0.83[EUR][1000 genomes] |
rs17677890 | 0.87[EUR][1000 genomes] |
rs17841357 | 0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1864229 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2079161 | 0.80[AFR][1000 genomes] |
rs2163068 | 0.89[EUR][1000 genomes] |
rs2358801 | 0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2905697 | 0.87[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2905699 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2914774 | 0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2914777 | 0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2914779 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2967232 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2967233 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2967234 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs2967240 | 0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs35005335 | 0.83[EUR][1000 genomes] |
rs4788646 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs55766519 | 0.87[EUR][1000 genomes] |
rs55808336 | 0.87[EUR][1000 genomes] |
rs56323671 | 0.91[EUR][1000 genomes] |
rs56347149 | 0.89[EUR][1000 genomes] |
rs56348767 | 0.89[EUR][1000 genomes] |
rs56389222 | 0.86[EUR][1000 genomes] |
rs56404261 | 0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs57220817 | 0.87[EUR][1000 genomes] |
rs58549165 | 0.87[EUR][1000 genomes] |
rs58745414 | 0.87[EUR][1000 genomes] |
rs58770834 | 0.89[EUR][1000 genomes] |
rs58860566 | 0.85[EUR][1000 genomes] |
rs60502114 | 0.85[EUR][1000 genomes] |
rs61475520 | 0.85[EUR][1000 genomes] |
rs62051486 | 0.92[EUR][1000 genomes] |
rs62051488 | 0.92[EUR][1000 genomes] |
rs62051497 | 0.84[EUR][1000 genomes] |
rs62052877 | 0.85[EUR][1000 genomes] |
rs62052878 | 0.84[EUR][1000 genomes] |
rs62052879 | 0.85[EUR][1000 genomes] |
rs62052880 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs62052881 | 0.85[EUR][1000 genomes] |
rs62052888 | 0.85[EUR][1000 genomes] |
rs62052890 | 0.87[EUR][1000 genomes] |
rs62052891 | 0.87[EUR][1000 genomes] |
rs62052895 | 0.87[EUR][1000 genomes] |
rs62052909 | 0.87[EUR][1000 genomes] |
rs62052911 | 0.87[EUR][1000 genomes] |
rs62052915 | 0.85[EUR][1000 genomes] |
rs62052920 | 0.90[EUR][1000 genomes] |
rs62052921 | 0.90[EUR][1000 genomes] |
rs62052923 | 0.82[EUR][1000 genomes] |
rs62052927 | 0.89[EUR][1000 genomes] |
rs62052954 | 0.86[EUR][1000 genomes] |
rs62054469 | 0.92[EUR][1000 genomes] |
rs62054470 | 0.92[EUR][1000 genomes] |
rs6499577 | 0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs7188640 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7189331 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7192221 | 0.89[EUR][1000 genomes] |
rs7193177 | 0.87[EUR][1000 genomes] |
rs7194470 | 0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs7194533 | 0.80[AFR][1000 genomes] |
rs7198233 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7198431 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7198788 | 0.89[EUR][1000 genomes] |
rs7199970 | 0.89[EUR][1000 genomes] |
rs7205109 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs72793252 | 0.85[EUR][1000 genomes] |
rs72793263 | 0.89[EUR][1000 genomes] |
rs72793266 | 0.90[EUR][1000 genomes] |
rs72793271 | 0.87[EUR][1000 genomes] |
rs8044665 | 0.82[EUR][1000 genomes] |
rs8046070 | 0.80[AFR][1000 genomes] |
rs8046749 | 0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs8048181 | 0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs8048832 | 0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs8049577 | 0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs8050815 | 0.91[EUR][1000 genomes] |
rs8059626 | 0.85[EUR][1000 genomes] |
rs8064129 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs877641 | 0.82[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs9302637 | 0.80[AFR][1000 genomes] |
rs9922217 | 0.80[AFR][1000 genomes];0.93[EUR][1000 genomes] |
rs9924296 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs9925470 | 0.87[EUR][1000 genomes] |
rs999697 | 0.89[EUR][1000 genomes] |
rs999698 | 0.89[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 | 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 |
6 | nsv1065173 | chr16:72509626-72693970 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
7 | nsv542951 | chr16:72509626-72693970 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | nsv1064027 | chr16:72559417-72656702 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
9 | nsv1063049 | chr16:72577004-72887111 | Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
10 | nsv542952 | chr16:72577004-72887111 | Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
11 | nsv1056987 | chr16:72620573-72658730 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
12 | nsv1064112 | chr16:72620573-72671503 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
13 | nsv1066815 | chr16:72627782-72658730 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
14 | nsv1055808 | chr16:72627782-72667298 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
15 | esv2751612 | chr16:72633299-72651914 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
16 | nsv431515 | chr16:72633299-72654499 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
17 | esv1818026 | chr16:72633305-72704680 | Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:72638400-72643600 | Weak transcription | GM12878-XiMat | blood |
2 | chr16:72639000-72643200 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
3 | chr16:72639000-72643400 | Weak transcription | H1 Cell Line | embryonic stem cell |
4 | chr16:72639200-72643000 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
5 | chr16:72639200-72643600 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
6 | chr16:72639400-72643400 | Weak transcription | HUES48 Cell Line | embryonic stem cell |