Variant report
Variant | rs7184224 |
---|---|
Chromosome Location | chr16:72654444-72654445 |
allele | C/T |
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 | chr16:72653301..72655444-chr16:72697417..72699415,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000259768 | Chromatin interaction |
ENSG00000261008 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11075927 | 1.00[AMR][1000 genomes] |
rs11075928 | 1.00[AMR][1000 genomes] |
rs11859210 | 1.00[AMR][1000 genomes] |
rs11861408 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11861672 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11863759 | 1.00[EUR][1000 genomes] |
rs11865496 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11866292 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12103150 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13329845 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13331987 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13332257 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13333424 | 1.00[AMR][1000 genomes] |
rs13336634 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13338662 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13339625 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1429069 | 1.00[AMR][1000 genomes] |
rs1429070 | 1.00[AMR][1000 genomes] |
rs16970897 | 1.00[AMR][1000 genomes] |
rs16970929 | 1.00[AMR][1000 genomes] |
rs16970996 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16971006 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16971145 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16971240 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2017748 | 1.00[AMR][1000 genomes] |
rs2053234 | 1.00[AMR][1000 genomes] |
rs2107154 | 1.00[AMR][1000 genomes] |
rs2189339 | 1.00[AMR][1000 genomes] |
rs2336436 | 1.00[AMR][1000 genomes] |
rs2840012 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28459407 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28464989 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28514442 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28568963 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28569075 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28616025 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28634932 | 1.00[AMR][1000 genomes] |
rs28693857 | 1.00[EUR][1000 genomes] |
rs28828717 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28847294 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4255793 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4624185 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55777547 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56991537 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57841266 | 1.00[AMR][1000 genomes] |
rs58363387 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58819288 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61192283 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6499589 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7184113 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7185566 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7187532 | 1.00[AMR][1000 genomes] |
rs7187768 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7192337 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7193704 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7195234 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7197250 | 1.00[AMR][1000 genomes] |
rs7199507 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7199594 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7203819 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73583171 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73583174 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73583188 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73583198 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73584928 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73584931 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73584955 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73590703 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73590712 | 1.00[EUR][1000 genomes] |
rs73590718 | 1.00[EUR][1000 genomes] |
rs73599411 | 1.00[AMR][1000 genomes] |
rs73601423 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73601436 | 1.00[AMR][1000 genomes] |
rs8043976 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8045319 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8045813 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8046375 | 1.00[AMR][1000 genomes] |
rs8048860 | 1.00[AMR][1000 genomes] |
rs8050489 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8051123 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8051420 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8051982 | 1.00[AMR][1000 genomes] |
rs8053288 | 1.00[AMR][1000 genomes] |
rs8053566 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8053837 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8057796 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8059369 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8061838 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9302636 | 1.00[AMR][1000 genomes] |
rs9302642 | 1.00[AMR][1000 genomes] |
rs9921921 | 1.00[AMR][1000 genomes] |
rs9923235 | 1.00[AMR][1000 genomes] |
rs9926141 | 1.00[AMR][1000 genomes] |
rs9926706 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9927677 | 1.00[AMR][1000 genomes] |
rs9928673 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9929006 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9932125 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9933062 | 1.00[AMR][1000 genomes] |
rs9933331 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9933418 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9934152 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9935400 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9935826 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9937525 | 0.85[AMR][1000 genomes] |
rs9938038 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | 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 |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | nsv1056987 | chr16:72620573-72658730 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
11 | 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 |
12 | nsv1066815 | chr16:72627782-72658730 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
13 | 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 |
14 | nsv431515 | chr16:72633299-72654499 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
15 | 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 |
16 | nsv1059111 | chr16:72647569-72751907 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:72643600-72660600 | Weak transcription | H1 Cell Line | embryonic stem cell |
2 | chr16:72644400-72660400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
3 | chr16:72646600-72659600 | Weak transcription | HepG2 | liver |
4 | chr16:72649600-72659600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
5 | chr16:72650400-72654600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |