Variant report
Variant | rs12098366 |
---|---|
Chromosome Location | chr10:46091616-46091617 |
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 |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000138293 | Chromatin interaction |
ENSG00000165507 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10508895 | 0.88[ASN][1000 genomes] |
rs10508896 | 1.00[ASN][1000 genomes] |
rs1060848 | 0.94[ASN][1000 genomes] |
rs11239526 | 0.80[ASN][1000 genomes] |
rs12761573 | 1.00[ASN][1000 genomes] |
rs12762495 | 0.94[ASN][1000 genomes] |
rs12763205 | 0.88[ASN][1000 genomes] |
rs12763285 | 1.00[ASN][1000 genomes] |
rs12764485 | 0.88[ASN][1000 genomes] |
rs12764652 | 0.88[ASN][1000 genomes] |
rs12764693 | 0.94[ASN][1000 genomes] |
rs12765244 | 1.00[ASN][1000 genomes] |
rs12766550 | 0.88[ASN][1000 genomes] |
rs12766764 | 1.00[ASN][1000 genomes] |
rs12768131 | 0.88[ASN][1000 genomes] |
rs12769244 | 0.88[ASN][1000 genomes] |
rs12771275 | 0.88[ASN][1000 genomes] |
rs12772102 | 1.00[ASN][1000 genomes] |
rs12772485 | 0.88[ASN][1000 genomes] |
rs12773263 | 0.88[ASN][1000 genomes] |
rs12773463 | 0.88[ASN][1000 genomes] |
rs12774453 | 1.00[ASN][1000 genomes] |
rs12774690 | 0.88[ASN][1000 genomes] |
rs12775527 | 0.94[ASN][1000 genomes] |
rs12776291 | 1.00[ASN][1000 genomes] |
rs12777172 | 1.00[ASN][1000 genomes] |
rs12778143 | 1.00[ASN][1000 genomes] |
rs12778980 | 0.88[ASN][1000 genomes] |
rs12779005 | 1.00[ASN][1000 genomes] |
rs12779198 | 0.94[ASN][1000 genomes] |
rs12779204 | 1.00[ASN][1000 genomes] |
rs12779281 | 0.88[ASN][1000 genomes] |
rs12779637 | 1.00[ASN][1000 genomes] |
rs12779976 | 1.00[ASN][1000 genomes] |
rs12781186 | 0.94[ASN][1000 genomes] |
rs12781506 | 1.00[ASN][1000 genomes] |
rs12783233 | 0.94[ASN][1000 genomes] |
rs17157798 | 0.88[ASN][1000 genomes] |
rs17157825 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs17157832 | 0.88[ASN][1000 genomes] |
rs17157836 | 0.88[ASN][1000 genomes] |
rs17157839 | 0.83[ASN][1000 genomes] |
rs17157852 | 0.88[ASN][1000 genomes] |
rs17157859 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17157861 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17157880 | 0.94[ASN][1000 genomes] |
rs17157884 | 0.94[ASN][1000 genomes] |
rs17157885 | 0.94[ASN][1000 genomes] |
rs17157887 | 0.94[ASN][1000 genomes] |
rs17157890 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs17157898 | 1.00[ASN][1000 genomes] |
rs17157919 | 1.00[ASN][1000 genomes] |
rs17157928 | 1.00[ASN][1000 genomes] |
rs17157931 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17157941 | 0.85[ASN][1000 genomes] |
rs17157944 | 0.85[ASN][1000 genomes] |
rs17157945 | 0.88[ASN][1000 genomes] |
rs17451208 | 1.00[ASN][1000 genomes] |
rs17523413 | 0.88[ASN][1000 genomes] |
rs17696005 | 0.88[ASN][1000 genomes] |
rs17696011 | 0.88[ASN][1000 genomes] |
rs17768650 | 0.85[ASN][1000 genomes] |
rs17768692 | 0.88[ASN][1000 genomes] |
rs2229136 | 0.88[ASN][1000 genomes] |
rs2279433 | 0.88[ASN][1000 genomes] |
rs2279434 | 0.88[ASN][1000 genomes] |
rs2288619 | 0.88[ASN][1000 genomes] |
rs33997730 | 0.91[ASN][1000 genomes] |
rs34011467 | 1.00[ASN][1000 genomes] |
rs34081402 | 0.88[ASN][1000 genomes] |
rs34081552 | 0.88[ASN][1000 genomes] |
rs34138033 | 1.00[ASN][1000 genomes] |
rs34144887 | 1.00[ASN][1000 genomes] |
rs34163035 | 1.00[ASN][1000 genomes] |
rs34176769 | 0.88[ASN][1000 genomes] |
rs34195613 | 1.00[ASN][1000 genomes] |
rs34268168 | 0.88[ASN][1000 genomes] |
rs34285816 | 0.88[ASN][1000 genomes] |
rs34309840 | 1.00[ASN][1000 genomes] |
rs34312822 | 0.88[ASN][1000 genomes] |
rs34383275 | 1.00[ASN][1000 genomes] |
rs34415465 | 0.88[ASN][1000 genomes] |
rs34516867 | 1.00[ASN][1000 genomes] |
rs34539215 | 1.00[ASN][1000 genomes] |
rs34566829 | 0.88[ASN][1000 genomes] |
rs34574958 | 1.00[ASN][1000 genomes] |
rs34604216 | 1.00[ASN][1000 genomes] |
rs34618850 | 1.00[ASN][1000 genomes] |
rs34654893 | 0.88[ASN][1000 genomes] |
rs34661476 | 0.88[ASN][1000 genomes] |
rs34663276 | 0.88[ASN][1000 genomes] |
rs34670342 | 1.00[ASN][1000 genomes] |
rs34731408 | 0.88[ASN][1000 genomes] |
rs34771643 | 0.88[ASN][1000 genomes] |
rs34793991 | 1.00[ASN][1000 genomes] |
rs34879733 | 0.82[ASN][1000 genomes] |
rs34897497 | 0.94[ASN][1000 genomes] |
rs34937315 | 0.88[ASN][1000 genomes] |
rs34960345 | 0.88[ASN][1000 genomes] |
rs35001302 | 1.00[ASN][1000 genomes] |
rs35003524 | 1.00[ASN][1000 genomes] |
rs35034867 | 1.00[ASN][1000 genomes] |
rs35036712 | 1.00[ASN][1000 genomes] |
rs35047800 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs35049879 | 1.00[ASN][1000 genomes] |
rs35070150 | 1.00[ASN][1000 genomes] |
rs35079443 | 0.88[ASN][1000 genomes] |
rs35081812 | 0.88[ASN][1000 genomes] |
rs35131026 | 0.94[ASN][1000 genomes] |
rs35150810 | 1.00[ASN][1000 genomes] |
rs35172875 | 0.88[ASN][1000 genomes] |
rs35183191 | 1.00[ASN][1000 genomes] |
rs35183751 | 1.00[ASN][1000 genomes] |
rs35187216 | 0.88[ASN][1000 genomes] |
rs35294227 | 0.88[ASN][1000 genomes] |
rs35303148 | 0.88[ASN][1000 genomes] |
rs35326978 | 0.88[ASN][1000 genomes] |
rs35331393 | 1.00[ASN][1000 genomes] |
rs35349326 | 0.88[ASN][1000 genomes] |
rs35356752 | 0.85[ASN][1000 genomes] |
rs35394192 | 0.88[ASN][1000 genomes] |
rs35410535 | 0.88[ASN][1000 genomes] |
rs35424022 | 0.88[ASN][1000 genomes] |
rs35464392 | 0.88[ASN][1000 genomes] |
rs35488254 | 0.88[ASN][1000 genomes] |
rs35504302 | 0.88[ASN][1000 genomes] |
rs35506889 | 1.00[ASN][1000 genomes] |
rs35585999 | 1.00[ASN][1000 genomes] |
rs35626777 | 1.00[ASN][1000 genomes] |
rs35629170 | 1.00[ASN][1000 genomes] |
rs35632234 | 0.88[ASN][1000 genomes] |
rs35639934 | 1.00[ASN][1000 genomes] |
rs35670420 | 1.00[ASN][1000 genomes] |
rs35713143 | 1.00[ASN][1000 genomes] |
rs35750365 | 0.94[ASN][1000 genomes] |
rs35775604 | 0.94[ASN][1000 genomes] |
rs35824277 | 1.00[ASN][1000 genomes] |
rs35902429 | 0.94[ASN][1000 genomes] |
rs35916836 | 1.00[ASN][1000 genomes] |
rs35918870 | 0.88[ASN][1000 genomes] |
rs35934513 | 1.00[ASN][1000 genomes] |
rs35968565 | 1.00[ASN][1000 genomes] |
rs36047811 | 0.88[ASN][1000 genomes] |
rs36052429 | 0.94[ASN][1000 genomes] |
rs36053776 | 1.00[ASN][1000 genomes] |
rs36054203 | 1.00[ASN][1000 genomes] |
rs36070535 | 0.88[ASN][1000 genomes] |
rs36070902 | 0.88[ASN][1000 genomes] |
rs36074276 | 1.00[ASN][1000 genomes] |
rs36100685 | 1.00[ASN][1000 genomes] |
rs36102549 | 0.94[ASN][1000 genomes] |
rs36109121 | 1.00[ASN][1000 genomes] |
rs3740109 | 0.88[ASN][1000 genomes] |
rs3740111 | 0.88[ASN][1000 genomes] |
rs3764990 | 0.88[ASN][1000 genomes] |
rs3802543 | 0.88[ASN][1000 genomes] |
rs3824616 | 0.88[ASN][1000 genomes] |
rs3824618 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs41301625 | 0.94[ASN][1000 genomes] |
rs41301629 | 0.88[ASN][1000 genomes] |
rs41301631 | 0.88[ASN][1000 genomes] |
rs4442500 | 1.00[ASN][1000 genomes] |
rs4576771 | 0.94[ASN][1000 genomes] |
rs60791882 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71494785 | 0.88[ASN][1000 genomes] |
rs71494786 | 0.88[ASN][1000 genomes] |
rs71494787 | 0.88[ASN][1000 genomes] |
rs71494788 | 0.88[ASN][1000 genomes] |
rs71494789 | 0.88[ASN][1000 genomes] |
rs71494790 | 0.88[ASN][1000 genomes] |
rs71494791 | 0.88[ASN][1000 genomes] |
rs71494792 | 0.88[ASN][1000 genomes] |
rs71494793 | 0.88[ASN][1000 genomes] |
rs71494794 | 0.88[ASN][1000 genomes] |
rs71494797 | 0.88[ASN][1000 genomes] |
rs71494798 | 0.88[ASN][1000 genomes] |
rs71494799 | 0.88[ASN][1000 genomes] |
rs71494800 | 0.88[ASN][1000 genomes] |
rs71496603 | 0.88[ASN][1000 genomes] |
rs71496605 | 0.88[ASN][1000 genomes] |
rs71496606 | 0.88[ASN][1000 genomes] |
rs71496607 | 0.88[ASN][1000 genomes] |
rs71496608 | 0.94[ASN][1000 genomes] |
rs71496609 | 0.94[ASN][1000 genomes] |
rs71496610 | 0.94[ASN][1000 genomes] |
rs71496611 | 0.94[ASN][1000 genomes] |
rs71496612 | 1.00[ASN][1000 genomes] |
rs71496613 | 1.00[ASN][1000 genomes] |
rs71496614 | 1.00[ASN][1000 genomes] |
rs71496618 | 1.00[ASN][1000 genomes] |
rs71496619 | 1.00[ASN][1000 genomes] |
rs71496620 | 0.88[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs71496621 | 1.00[ASN][1000 genomes] |
rs71496622 | 1.00[ASN][1000 genomes] |
rs71496623 | 1.00[ASN][1000 genomes] |
rs71496624 | 1.00[ASN][1000 genomes] |
rs71496625 | 1.00[ASN][1000 genomes] |
rs71499565 | 0.88[ASN][1000 genomes] |
rs71499566 | 0.88[ASN][1000 genomes] |
rs71499567 | 1.00[ASN][1000 genomes] |
rs71515355 | 0.88[ASN][1000 genomes] |
rs73291113 | 1.00[EUR][1000 genomes] |
rs73291115 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73291121 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73291122 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73291195 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73291198 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs768673 | 0.88[ASN][1000 genomes] |
rs7898761 | 0.94[ASN][1000 genomes] |
rs901682 | 0.88[ASN][1000 genomes] |
rs901683 | 0.88[ASN][1000 genomes] |
rs901684 | 0.88[ASN][1000 genomes] |
rs9422439 | 1.00[ASN][1000 genomes] |
rs9422440 | 1.00[ASN][1000 genomes] |
rs9422441 | 1.00[ASN][1000 genomes] |
rs9422442 | 1.00[ASN][1000 genomes] |
rs9422647 | 0.88[ASN][1000 genomes] |
rs9422650 | 1.00[ASN][1000 genomes] |
rs9422651 | 1.00[ASN][1000 genomes] |
rs9422652 | 1.00[ASN][1000 genomes] |
rs9422653 | 1.00[ASN][1000 genomes] |
rs9422654 | 1.00[ASN][1000 genomes] |
rs9422655 | 1.00[ASN][1000 genomes] |
rs9422657 | 1.00[ASN][1000 genomes] |
rs9422658 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv430166 | chr10:45668894-46148794 | Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
2 | nsv993428 | chr10:45742877-46224333 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
3 | nsv895108 | chr10:45878908-46224333 | Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
4 | nsv895109 | chr10:45882741-46210665 | Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
5 | nsv895112 | chr10:46012620-46202216 | Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
6 | nsv1050880 | chr10:46091441-46160597 | Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
7 | nsv540588 | chr10:46091441-46160597 | ZNF genes & repeats Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:46090400-46092600 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
2 | chr10:46090400-46094200 | Weak transcription | Small Intestine | intestine |
3 | chr10:46090600-46167600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr10:46090800-46092800 | Enhancers | Fetal Intestine Small | intestine |
5 | chr10:46090800-46094800 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
6 | chr10:46090800-46095800 | Enhancers | Fetal Intestine Large | intestine |
7 | chr10:46090800-46096000 | Weak transcription | Right Ventricle | heart |
8 | chr10:46091000-46092800 | Enhancers | HepG2 | liver |
9 | chr10:46091000-46094000 | Weak transcription | Liver | Liver |
10 | chr10:46091000-46094400 | Weak transcription | K562 | blood |
11 | chr10:46091000-46095600 | Weak transcription | Duodenum Mucosa | Duodenum |
12 | chr10:46091600-46091800 | Enhancers | Rectal Mucosa Donor 29 | rectum |