Variant report
Variant | rs13261725 |
---|---|
Chromosome Location | chr8:91866297-91866298 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:7)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:7 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:91852622..91854698-chr8:91866211..91868646,2 | MCF-7 | breast: | |
2 | chr8:91866235..91867984-chr8:91868393..91871249,2 | MCF-7 | breast: | |
3 | chr8:91865391..91867140-chr8:91886404..91889323,2 | MCF-7 | breast: | |
4 | chr8:91866002..91867663-chr8:91923726..91925814,2 | MCF-7 | breast: | |
5 | chr8:91864776..91867675-chr8:91910571..91913106,2 | K562 | blood: | |
6 | chr8:91858625..91861486-chr8:91864590..91867170,2 | MCF-7 | breast: | |
7 | chr8:91866110..91869970-chr8:91870165..91874057,7 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000254251 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10086609 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10090389 | 0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10108616 | 0.89[EUR][1000 genomes] |
rs1011254 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs10808631 | 0.87[EUR][1000 genomes] |
rs10956779 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10956780 | 0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10956781 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10956782 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10956784 | 0.86[EUR][1000 genomes] |
rs10956785 | 0.89[EUR][1000 genomes] |
rs1125229 | 0.89[EUR][1000 genomes] |
rs12542103 | 0.86[EUR][1000 genomes] |
rs12548099 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12548141 | 0.84[EUR][1000 genomes] |
rs12549909 | 0.89[EUR][1000 genomes] |
rs12550756 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12675931 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13264873 | 0.89[EUR][1000 genomes] |
rs13268798 | 0.86[EUR][1000 genomes] |
rs13279759 | 0.88[EUR][1000 genomes] |
rs1354517 | 0.87[EUR][1000 genomes] |
rs1354518 | 0.88[EUR][1000 genomes] |
rs1354519 | 0.86[EUR][1000 genomes] |
rs1354520 | 0.86[EUR][1000 genomes] |
rs1386107 | 0.89[EUR][1000 genomes] |
rs1386108 | 0.89[EUR][1000 genomes] |
rs1386109 | 0.86[EUR][1000 genomes] |
rs1386112 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs1394501 | 0.84[EUR][1000 genomes] |
rs1394502 | 0.84[EUR][1000 genomes] |
rs1463920 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1486465 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1486466 | 0.87[EUR][1000 genomes] |
rs1504787 | 0.89[EUR][1000 genomes] |
rs1504789 | 0.84[EUR][1000 genomes] |
rs1504790 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1504795 | 0.86[EUR][1000 genomes] |
rs1504796 | 0.89[EUR][1000 genomes] |
rs1604917 | 0.87[EUR][1000 genomes] |
rs1604918 | 0.85[EUR][1000 genomes] |
rs1604919 | 0.88[EUR][1000 genomes] |
rs16905444 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs16905567 | 0.87[EUR][1000 genomes] |
rs16905571 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1857752 | 0.88[EUR][1000 genomes] |
rs1910726 | 0.89[EUR][1000 genomes] |
rs1910727 | 0.89[EUR][1000 genomes] |
rs1982785 | 0.87[EUR][1000 genomes] |
rs1984428 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2062880 | 0.84[EUR][1000 genomes] |
rs2129260 | 0.87[EUR][1000 genomes] |
rs2631012 | 0.83[EUR][1000 genomes] |
rs2631014 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs34480586 | 0.85[EUR][1000 genomes] |
rs34637621 | 0.87[EUR][1000 genomes] |
rs35234301 | 0.88[EUR][1000 genomes] |
rs35918434 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs3890611 | 0.89[EUR][1000 genomes] |
rs4416793 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4452761 | 0.90[ASN][1000 genomes] |
rs4517081 | 0.86[EUR][1000 genomes] |
rs4735414 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4735415 | 0.90[ASN][1000 genomes] |
rs4735416 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4735417 | 0.89[EUR][1000 genomes] |
rs4735418 | 0.88[EUR][1000 genomes] |
rs4735419 | 0.87[EUR][1000 genomes] |
rs4735428 | 0.87[EUR][1000 genomes] |
rs55735096 | 0.81[EUR][1000 genomes] |
rs6471257 | 0.85[EUR][1000 genomes] |
rs6471258 | 0.86[EUR][1000 genomes] |
rs6471259 | 0.89[EUR][1000 genomes] |
rs6471260 | 0.86[EUR][1000 genomes] |
rs6471261 | 0.87[EUR][1000 genomes] |
rs6471262 | 0.87[EUR][1000 genomes] |
rs67320710 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6986276 | 0.88[EUR][1000 genomes] |
rs6993462 | 0.84[EUR][1000 genomes] |
rs6994971 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6999838 | 0.87[EUR][1000 genomes] |
rs7002244 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7003020 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7006384 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7014480 | 0.84[EUR][1000 genomes] |
rs7813402 | 0.87[EUR][1000 genomes] |
rs7821107 | 0.83[EUR][1000 genomes] |
rs7829663 | 0.83[EUR][1000 genomes] |
rs7830264 | 0.84[EUR][1000 genomes] |
rs901382 | 0.87[EUR][1000 genomes] |
rs937738 | 0.86[EUR][1000 genomes] |
rs937739 | 0.89[EUR][1000 genomes] |
rs9643317 | 0.84[EUR][1000 genomes] |
rs9969519 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028628 | chr8:91680968-92418954 | Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
2 | nsv539672 | chr8:91680968-92418954 | Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:91857400-91871000 | Weak transcription | Brain Cingulate Gyrus | brain |
2 | chr8:91860200-91870800 | Weak transcription | Brain Inferior Temporal Lobe | brain |
3 | chr8:91863000-91880600 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
4 | chr8:91865000-91866400 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
5 | chr8:91865600-91871400 | Weak transcription | Brain Hippocampus Middle | brain |