Variant report
Variant | rs73599301 |
---|---|
Chromosome Location | chr16:81149182-81149183 |
allele | C/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 | chr16:81149124..81150808-chr16:81152583..81155563,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10400998 | 1.00[ASN][1000 genomes] |
rs10468366 | 1.00[ASN][1000 genomes] |
rs13332317 | 1.00[ASN][1000 genomes] |
rs13332530 | 1.00[ASN][1000 genomes] |
rs16954525 | 0.92[ASN][1000 genomes] |
rs16954528 | 1.00[ASN][1000 genomes] |
rs16954688 | 1.00[ASN][1000 genomes] |
rs1869347 | 1.00[ASN][1000 genomes] |
rs2549901 | 1.00[ASN][1000 genomes] |
rs28469459 | 1.00[ASN][1000 genomes] |
rs28472979 | 1.00[ASN][1000 genomes] |
rs28586999 | 1.00[ASN][1000 genomes] |
rs28709530 | 1.00[ASN][1000 genomes] |
rs4889239 | 0.80[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs55648346 | 1.00[ASN][1000 genomes] |
rs55664147 | 0.84[ASN][1000 genomes] |
rs55894951 | 1.00[ASN][1000 genomes] |
rs56117555 | 1.00[ASN][1000 genomes] |
rs56333013 | 0.84[ASN][1000 genomes] |
rs56378007 | 1.00[ASN][1000 genomes] |
rs56758545 | 0.84[ASN][1000 genomes] |
rs56838270 | 0.84[ASN][1000 genomes] |
rs57435835 | 0.92[ASN][1000 genomes] |
rs57687812 | 1.00[ASN][1000 genomes] |
rs57830624 | 0.84[ASN][1000 genomes] |
rs57906343 | 1.00[ASN][1000 genomes] |
rs58418167 | 1.00[ASN][1000 genomes] |
rs60573779 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs61435632 | 1.00[ASN][1000 genomes] |
rs61438195 | 1.00[ASN][1000 genomes] |
rs61495305 | 1.00[ASN][1000 genomes] |
rs6564815 | 0.84[ASN][1000 genomes] |
rs6564816 | 0.84[ASN][1000 genomes] |
rs7187063 | 0.84[ASN][1000 genomes] |
rs7194808 | 1.00[ASN][1000 genomes] |
rs7195463 | 1.00[ASN][1000 genomes] |
rs7197019 | 1.00[ASN][1000 genomes] |
rs7198494 | 0.92[ASN][1000 genomes] |
rs72827277 | 1.00[ASN][1000 genomes] |
rs73597275 | 0.89[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs74028898 | 0.84[ASN][1000 genomes] |
rs74028901 | 0.84[ASN][1000 genomes] |
rs74028902 | 0.92[ASN][1000 genomes] |
rs74030503 | 0.92[ASN][1000 genomes] |
rs74030505 | 1.00[ASN][1000 genomes] |
rs8045625 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8061024 | 1.00[ASN][1000 genomes] |
rs8061203 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8062432 | 1.00[ASN][1000 genomes] |
rs8177847 | 1.00[ASN][1000 genomes] |
rs8177854 | 1.00[ASN][1000 genomes] |
rs8177857 | 1.00[ASN][1000 genomes] |
rs8177858 | 1.00[ASN][1000 genomes] |
rs8177859 | 1.00[ASN][1000 genomes] |
rs8177860 | 1.00[ASN][1000 genomes] |
rs8177868 | 1.00[ASN][1000 genomes] |
rs8177869 | 1.00[ASN][1000 genomes] |
rs8177870 | 1.00[ASN][1000 genomes] |
rs8177871 | 1.00[ASN][1000 genomes] |
rs8177872 | 1.00[ASN][1000 genomes] |
rs8177873 | 1.00[ASN][1000 genomes] |
rs8177874 | 1.00[ASN][1000 genomes] |
rs8177877 | 1.00[ASN][1000 genomes] |
rs8177879 | 1.00[ASN][1000 genomes] |
rs8177881 | 1.00[ASN][1000 genomes] |
rs8177890 | 1.00[ASN][1000 genomes] |
rs8177893 | 1.00[ASN][1000 genomes] |
rs8177895 | 1.00[ASN][1000 genomes] |
rs8177905 | 1.00[ASN][1000 genomes] |
rs8177907 | 1.00[ASN][1000 genomes] |
rs8177908 | 1.00[ASN][1000 genomes] |
rs8177910 | 1.00[ASN][1000 genomes] |
rs8177913 | 1.00[ASN][1000 genomes] |
rs8177914 | 1.00[ASN][1000 genomes] |
rs8177915 | 1.00[ASN][1000 genomes] |
rs8177917 | 1.00[ASN][1000 genomes] |
rs8177922 | 1.00[ASN][1000 genomes] |
rs8177924 | 1.00[ASN][1000 genomes] |
rs8177926 | 1.00[ASN][1000 genomes] |
rs8177927 | 1.00[ASN][1000 genomes] |
rs8177928 | 1.00[ASN][1000 genomes] |
rs8177929 | 1.00[ASN][1000 genomes] |
rs8177930 | 0.92[ASN][1000 genomes] |
rs8177932 | 1.00[ASN][1000 genomes] |
rs8177933 | 1.00[ASN][1000 genomes] |
rs8177934 | 1.00[ASN][1000 genomes] |
rs8177935 | 1.00[ASN][1000 genomes] |
rs8177936 | 1.00[ASN][1000 genomes] |
rs8177937 | 1.00[ASN][1000 genomes] |
rs8177941 | 1.00[ASN][1000 genomes] |
rs8177949 | 1.00[ASN][1000 genomes] |
rs9932197 | 1.00[ASN][1000 genomes] |
rs9934205 | 0.85[ASN][1000 genomes] |
rs9934220 | 1.00[ASN][1000 genomes] |
rs9935938 | 1.00[ASN][1000 genomes] |
rs9937014 | 1.00[ASN][1000 genomes] |
rs9937594 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948534 | chr16:80867635-81160492 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 55 gene(s) | inside rSNPs | diseases |
2 | nsv532569 | chr16:80980356-81700149 | Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 71 gene(s) | inside rSNPs | diseases |
3 | nsv532597 | chr16:81009718-81388348 | Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
4 | nsv427984 | chr16:81026691-81320341 | Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
5 | esv2422360 | chr16:81066033-81180727 | Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
6 | esv2751615 | chr16:81093099-81307599 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
7 | nsv530715 | chr16:81117168-81252875 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
8 | nsv907005 | chr16:81121353-81194912 | Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
9 | nsv1067144 | chr16:81129298-81181641 | Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
10 | nsv1059006 | chr16:81139073-81155094 | Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
11 | nsv1063460 | chr16:81139073-81157385 | Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
12 | nsv520035 | chr16:81145675-81157521 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS | TF binding regionChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:81130000-81187600 | Weak transcription | Right Atrium | heart |
2 | chr16:81141200-81156600 | Weak transcription | Brain Angular Gyrus | brain |
3 | chr16:81141200-81169600 | Weak transcription | Brain Anterior Caudate | brain |
4 | chr16:81141400-81150800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr16:81141400-81153800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr16:81141400-81169600 | Weak transcription | Brain Cingulate Gyrus | brain |
7 | chr16:81141400-81169600 | Weak transcription | Brain Hippocampus Middle | brain |
8 | chr16:81147800-81156800 | Weak transcription | Adipose Nuclei | Adipose |
9 | chr16:81149000-81149400 | Enhancers | Fetal Heart | heart |