Variant report
Variant | rs7701404 |
---|---|
Chromosome Location | chr5:29149243-29149244 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:5)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:5 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | MAFF | chr5:29149126-29149326 | HepG2 | liver: | n/a | chr5:29149237-29149255 |
2 | MAFK | chr5:29149083-29149325 | IMR90 | lung: | n/a | chr5:29149239-29149254 chr5:29149239-29149250 chr5:29149239-29149250 |
3 | MAFK | chr5:29149100-29149290 | HepG2 | liver: | n/a | chr5:29149239-29149254 chr5:29149239-29149250 chr5:29149239-29149250 |
4 | MAFK | chr5:29149083-29149378 | HepG2 | liver: | n/a | chr5:29149239-29149254 chr5:29149239-29149250 chr5:29149239-29149250 |
5 | MAFF | chr5:29149112-29149348 | K562 | blood: | n/a | chr5:29149237-29149255 |
No data |
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No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000259786 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10037010 | 0.81[ASN][1000 genomes] |
rs10037061 | 0.81[ASN][1000 genomes] |
rs10038700 | 0.81[ASN][1000 genomes] |
rs10039602 | 0.81[ASN][1000 genomes] |
rs10039668 | 0.81[ASN][1000 genomes] |
rs10039689 | 0.81[ASN][1000 genomes] |
rs10039720 | 0.81[ASN][1000 genomes] |
rs10040911 | 0.81[ASN][1000 genomes] |
rs10042518 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10043330 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10045742 | 0.81[ASN][1000 genomes] |
rs10050492 | 0.81[ASN][1000 genomes] |
rs10056451 | 0.81[ASN][1000 genomes] |
rs10056682 | 0.81[ASN][1000 genomes] |
rs10057831 | 0.81[ASN][1000 genomes] |
rs10057922 | 0.81[ASN][1000 genomes] |
rs10058093 | 0.81[ASN][1000 genomes] |
rs10058226 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10058284 | 0.81[ASN][1000 genomes] |
rs10064605 | 0.81[ASN][1000 genomes] |
rs10064724 | 0.81[ASN][1000 genomes] |
rs10064739 | 0.81[ASN][1000 genomes] |
rs10064857 | 0.81[ASN][1000 genomes] |
rs10064882 | 0.81[ASN][1000 genomes] |
rs10064929 | 0.81[ASN][1000 genomes] |
rs10064947 | 0.81[ASN][1000 genomes] |
rs10065134 | 0.81[ASN][1000 genomes] |
rs10065602 | 0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10066074 | 0.81[ASN][1000 genomes] |
rs10066078 | 0.81[ASN][1000 genomes] |
rs10066277 | 0.81[ASN][1000 genomes] |
rs10068481 | 0.81[ASN][1000 genomes] |
rs10071241 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10072095 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10072535 | 0.81[ASN][1000 genomes] |
rs10072954 | 0.81[ASN][1000 genomes] |
rs10072999 | 0.81[ASN][1000 genomes] |
rs10073201 | 0.81[ASN][1000 genomes] |
rs10074755 | 0.81[ASN][1000 genomes] |
rs10079924 | 0.81[ASN][1000 genomes] |
rs10080202 | 0.81[ASN][1000 genomes] |
rs10440641 | 0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10472145 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10472151 | 0.81[ASN][1000 genomes] |
rs10472154 | 0.81[ASN][1000 genomes] |
rs10472678 | 0.81[ASN][1000 genomes] |
rs10472680 | 0.81[ASN][1000 genomes] |
rs10472681 | 0.81[ASN][1000 genomes] |
rs11742838 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12109506 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12697209 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13164231 | 0.81[ASN][1000 genomes] |
rs13182294 | 0.81[ASN][1000 genomes] |
rs13356879 | 0.81[ASN][1000 genomes] |
rs13357238 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13359197 | 0.81[ASN][1000 genomes] |
rs1478863 | 0.81[ASN][1000 genomes] |
rs1587207 | 0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28637428 | 0.81[ASN][1000 genomes] |
rs309666 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs309670 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34302105 | 0.81[ASN][1000 genomes] |
rs34426391 | 0.81[ASN][1000 genomes] |
rs34687289 | 0.81[ASN][1000 genomes] |
rs34979719 | 0.81[ASN][1000 genomes] |
rs35746880 | 0.81[ASN][1000 genomes] |
rs3853229 | 0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs3886358 | 0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4130798 | 0.81[ASN][1000 genomes] |
rs4130799 | 0.81[ASN][1000 genomes] |
rs4130800 | 0.81[ASN][1000 genomes] |
rs4374768 | 0.81[ASN][1000 genomes] |
rs4398647 | 0.81[ASN][1000 genomes] |
rs4631192 | 0.81[ASN][1000 genomes] |
rs55882562 | 0.92[ASN][1000 genomes] |
rs62352828 | 0.81[ASN][1000 genomes] |
rs62352850 | 0.81[ASN][1000 genomes] |
rs62352851 | 0.81[ASN][1000 genomes] |
rs631844 | 0.89[ASN][1000 genomes] |
rs6450669 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6450670 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6450673 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6866060 | 0.81[ASN][1000 genomes] |
rs6873888 | 0.81[ASN][1000 genomes] |
rs6885342 | 0.81[ASN][1000 genomes] |
rs6899088 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7444084 | 0.81[ASN][1000 genomes] |
rs7714444 | 0.81[ASN][1000 genomes] |
rs7714882 | 0.81[ASN][1000 genomes] |
rs7715935 | 0.81[ASN][1000 genomes] |
rs7722678 | 0.81[ASN][1000 genomes] |
rs7731764 | 0.81[ASN][1000 genomes] |
rs7732750 | 0.81[ASN][1000 genomes] |
rs7732811 | 0.81[ASN][1000 genomes] |
rs7733592 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7737230 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9292297 | 0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9292307 | 0.81[ASN][1000 genomes] |
rs9292311 | 0.81[ASN][1000 genomes] |
rs9292312 | 0.81[ASN][1000 genomes] |
rs9292314 | 0.81[ASN][1000 genomes] |
rs9986176 | 0.81[ASN][1000 genomes] |
rs9986231 | 0.81[ASN][1000 genomes] |
rs9986285 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023990 | chr5:28917253-29220447 | Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
2 | esv3528360 | chr5:29069255-29548659 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
3 | esv3528361 | chr5:29069255-29548659 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
4 | nsv1022253 | chr5:29076460-29195987 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
5 | nsv1016603 | chr5:29102713-29843965 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 43 gene(s) | inside rSNPs | diseases |
6 | nsv537712 | chr5:29102713-29843965 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 43 gene(s) | inside rSNPs | diseases |
7 | nsv1030526 | chr5:29125802-29204186 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
8 | nsv964827 | chr5:29138557-29198352 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:29144000-29150600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr5:29146800-29150600 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
3 | chr5:29148000-29151400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
4 | chr5:29148400-29149400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
5 | chr5:29148600-29151400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
6 | chr5:29148800-29150800 | Enhancers | HUES6 Cell Line | embryonic stem cell |
7 | chr5:29148800-29151000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
8 | chr5:29149000-29149600 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
9 | chr5:29149000-29150200 | Weak transcription | H1 Cell Line | embryonic stem cell |
10 | chr5:29149000-29150200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
11 | chr5:29149000-29151600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
12 | chr5:29149200-29153400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |